Canonical Allele Identifier: PA177369
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164665
ClinVar RCV Id: RCV000151483 RCV001075256 RCV001109644 RCV001109643 RCV001109642 RCV001514137
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg336Cys
CA177368
NM_000260.4:c.1006C>T