Canonical Allele Identifier: PA916029060
Gene: TPMT HGNC NCBI

Linked Data

ClinVar Variation Id: 12721
ClinVar RCV Id: RCV000013558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333747.1:p.Ala80Pro
CA122644
NM_001346818.1:c.238G>C