Canonical Allele Identifier: PA3088572938
Gene: COMT HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000745.1:p.Gln73His
CA410688825
NM_000754.4:c.219G>C
CA410688827
NM_000754.4:c.219G>T