Amino acid replacement: I571T.
The I571T change is equivalent to a I592T change in the orthologous human ATP1A1 gene, a variant associated with Charcot-Marie-Tooth disease type 2.
T20965582C
I610T | Atpalpha-PA; I571T | Atpalpha-PB; I571T | Atpalpha-PC; I571T | Atpalpha-PD; I571T | Atpalpha-PE; I571T | Atpalpha-PF; I571T | Atpalpha-PG; I571T | Atpalpha-PH; I571T | Atpalpha-PI; I571T | Atpalpha-PJ; I571T | Atpalpha-PK
I571T
Analogous mutation in human ATP1A1 implicated in Charcot-Marie-Tooth disease type 2; mutation carried on in vitro construct; site of nucleotide substitution in fly gene inferred by FlyBase curator based on reported amino acid change.