Canonical Allele Identifier: PA2573180461
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1374847
ClinVar RCV Id: RCV001879361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Val469Met
CA6197493
NM_001127180.2:c.1405G>A