Canonical Allele Identifier: PA2825627922
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1303075
ClinVar RCV Id: RCV001756574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.His1976Arg
CA381934726
NM_001127180.2:c.5927A>G