Canonical Allele Identifier: PA915980862
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 636221
ClinVar RCV Id: RCV000787915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gln613Arg
CA381938324
NM_001127180.2:c.1838A>G