Canonical Allele Identifier: PA2825114867
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1500753
ClinVar RCV Id: RCV002015891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Tyr298Asn
CA381932917
NM_000260.4:c.892T>A