Canonical Allele Identifier: PA2829712088
Gene: COMT HGNC NCBI

Linked Data

ClinVar Variation Id: 17591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009294.1:p.Val108Met
CA127287
NM_007310.3:c.322G>A