Canonical Allele Identifier: PA2829896414
Gene: UGT1A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2161778
ClinVar RCV Id: RCV003078743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061950.2:p.Glu460Asp
CA2180113
NM_019077.3:c.1380G>C
CA351076195
NM_019077.3:c.1380G>T