Allele Registry

Canonical Allele Identifier: PA2829712094

Gene: COMT HGNC NCBI

ClinVar RCV:

RCV001028871

ClinVar Variation:

828957

HGVS (amino-acid)	Matching Registered Transcripts
NP_009294.1:p.Ala118Val	CA10104633 NM_007310.3:c.353C>T