Allele Registry

Canonical Allele Identifier: PA127288

Gene: COMT HGNC NCBI

ClinVar RCV:

RCV000019156

RCV000244083

RCV001028880

RCV003633481

ClinVar Variation:

17591

HGVS (amino-acid)	Matching Registered Transcripts
NP_000745.1:p.Val158Met	CA127287 NM_000754.4:c.472G>A