Allele Registry

Canonical Allele Identifier: PA1139699297

Gene: DPYD HGNC NCBI

ClinVar Allele:

864899

ClinVar RCV:

RCV001096821

RCV002554903

ClinVar Variation:

874135

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Thr760Ile	CA963080 NM_000110.4:c.2279C>T