Canonical Allele Identifier: PA2825789354
Gene: COMT HGNC NCBI

Linked Data

ClinVar Variation Id: 828957
ClinVar RCV Id: RCV001028871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128634.1:p.Ala168Val
CA10104633
NM_001135162.2:c.503C>T