Canonical Allele Identifier: PA122082
Gene: UGT1A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 12281
ClinVar RCV Id: RCV000013074 RCV000013073 RCV000147900 RCV000763480 RCV000999563 RCV001810853 RCV004540998
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_995584.1:p.Tyr218Asp
CA122080
NM_205862.3:c.652T>G