Canonical Allele Identifier: PA2825115727
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1314131
ClinVar RCV Id: RCV001771362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Tyr696Cys
CA381939562
NM_000260.4:c.2087A>G