Canonical Allele Identifier: PA2825789335
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_001128634.1:p.Ala72Ser
CA127289
NM_001135162.2:c.214G>T