Canonical Allele Identifier: PA2573065512
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1314131
ClinVar RCV Id: RCV001771362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Tyr696Cys
CA381939562
NM_001127180.2:c.2087A>G