Canonical Allele Identifier: PA2829896120
Gene: UGT1A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2161778
ClinVar RCV Id: RCV003078743
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061949.3:p.Glu460Asp
CA2180113
NM_019076.5:c.1380G>C
CA351076195
NM_019076.5:c.1380G>T