Canonical Allele Identifier: PA100085
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 2429760
ClinVar RCV Id: RCV003127213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000252.1:p.Pro274Arg
CA343725980
NM_000261.2:c.821C>G