Allele Registry

Canonical Allele Identifier: PA2825789307

Gene: COMT HGNC NCBI

ClinVar RCV:

RCV001028871

ClinVar Variation:

828957

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128633.1:p.Ala168Val	CA10104633 NM_001135161.2:c.503C>T