Allele Registry

Canonical Allele Identifier: PA100075

Gene: MYOC HGNC NCBI

ClinVar Variation Id: 1723163

ClinVar RCV Id: RCV002306263

ClinVar Variation Id: 2498112

ClinVar RCV Id: RCV003219173

HGVS (amino-acid)	Matching Registered Transcripts
NP_000252.1:p.Phe369Leu	CA343724698 NM_000261.2:c.1107C>G CA343724699 NM_000261.2:c.1107C>A CA343724711 NM_000261.2:c.1105T>C