Allele Registry

Canonical Allele Identifier: PA2825789287

Gene: COMT HGNC NCBI

ClinVar RCV:

RCV000019157

RCV001028887

ClinVar Variation:

17592

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128633.1:p.Ala72Ser	CA127289 NM_001135161.2:c.214G>T