Canonical Allele Identifier: PA2825115171
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1374847
ClinVar RCV Id: RCV001879361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Val469Met
CA6197493
NM_000260.4:c.1405G>A