Canonical Allele Identifier: PA100170
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 1686794
ClinVar RCV Id: RCV002248299
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000252.1:p.Ser502Pro
CA343722794
NM_000261.2:c.1504T>C