Allele Registry

Canonical Allele Identifier: PA658825235

Gene: DPYD HGNC NCBI

ClinVar Allele:

541349

ClinVar RCV:

RCV000670232

RCV002532097

RCV003330887

ClinVar Variation:

554571

HGVS (amino-acid)	Matching Registered Transcripts
NP_000101.2:p.Tyr211Cys	CA963604 NM_000110.4:c.632A>G