Canonical Allele Identifier: PA2829712041
Gene: COMT HGNC NCBI

Linked Data

ClinVar Variation Id: 17592
ClinVar RCV Id: RCV000019157 RCV001028887
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009294.1:p.Ala22Ser
CA127289
NM_007310.3:c.64G>T