Canonical Allele Identifier: PA2829969102
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1301539
ClinVar RCV Id: RCV001733511 RCV001810752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Asp356Asn
CA2179984
NM_021027.3:c.1066G>A