Canonical Allele Identifier: PA2828320616
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Glu1159Lys
CA278649
NM_001369365.1:c.3475G>A