Canonical Allele Identifier: PA2829969139
Gene: UGT1A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 597250
ClinVar RCV Id: RCV000733308
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066307.1:p.Pro384Arg
CA351074205
NM_021027.3:c.1151C>G
CA913189479
NM_021027.3:c.1151_1152delinsGT