Canonical Allele Identifier: PA100139
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 1439558
ClinVar RCV Id: RCV001965333 RCV003126018
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000252.1:p.Ser341Pro
CA343725060
NM_000261.2:c.1021T>C