Canonical Allele Identifier: PA100149
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 1723164
ClinVar RCV Id: RCV002306264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000252.1:p.Ser393Arg
CA32685671
NM_000261.2:c.1179C>G
CA343724406
NM_000261.2:c.1179C>A
CA343724416
NM_000261.2:c.1177A>C