Canonical Allele Identifier: PA100023
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 2570620
ClinVar RCV Id: RCV003307380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000252.1:p.Ile465Met
CA343723421
NM_000261.2:c.1395C>G