Canonical Allele Identifier: PA114026
Gene: DPYS HGNC NCBI
ClinVar RCV:
RCV000000210
ClinVar Variation:
187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376.1:p.Arg412Met
CA114025
NM_001385.3:c.1235G>T