Canonical Allele Identifier: PA2828319634
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2142562
ClinVar RCV Id: RCV003076342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Lys309Arg
CA6197311
NM_001369365.1:c.926A>G