Canonical Allele Identifier: PA1139679903
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 983065
ClinVar RCV Id: RCV001262911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg668Leu
CA381939293
NM_001127180.2:c.2003G>T