Allele Registry

Canonical Allele Identifier: PA2829712088

Gene: COMT HGNC NCBI

ClinVar RCV:

RCV000019156

RCV000244083

RCV001028880

RCV003633481

ClinVar Variation:

17591

HGVS (amino-acid)	Matching Registered Transcripts
NP_009294.1:p.Val108Met	CA127287 NM_007310.3:c.322G>A