Canonical Allele Identifier: PA915980886
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 802706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg634Gln
CA6197634
NM_001127180.2:c.1901G>A