Allele Registry

Canonical Allele Identifier: PA913193269

Gene: UGT1A1 HGNC NCBI

ClinVar RCV:

RCV000729304

ClinVar Variation:

594091

HGVS (amino-acid)	Matching Registered Transcripts
NP_000454.1:p.Asn400His	CA67596366 NM_000463.3:c.1198A>C