Canonical Allele Identifier: PA2827385918
Gene: TPMT HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333746.1:p.Ala80Pro
CA122644
NM_001346817.1:c.238G>C