Canonical Allele Identifier: PA2828319812
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1374847
ClinVar RCV Id: RCV001879361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Val458Met
CA6197493
NM_001369365.1:c.1372G>A