Canonical Allele Identifier: PA916043507
Gene: COMT HGNC NCBI

Linked Data

ClinVar Variation Id: 17592
ClinVar RCV Id: RCV000019157 RCV001028887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349757.1:p.Ala72Ser
CA127289
NM_001362828.2:c.214G>T