Canonical Allele Identifier: PA2829896360
Gene: UGT1A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 597250
ClinVar RCV Id: RCV000733308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061950.2:p.Pro384Arg
CA351074205
NM_019077.3:c.1151C>G
CA913189479
NM_019077.3:c.1151_1152delinsGT