Canonical Allele Identifier: PA645486318
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 287480
ClinVar RCV Id: RCV000281091 RCV000671369 RCV001788190 RCV002518984 RCV003920127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000101.2:p.Thr768Lys
CA963062
NM_000110.4:c.2303C>A