Canonical Allele Identifier: PA2825114851
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1434426
ClinVar RCV Id: RCV001984638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly284Val
CA6197287
NM_000260.4:c.851G>T