Canonical Allele Identifier: PA645510262
Gene: UGT1A7 HGNC NCBI

Linked Data

ClinVar Variation Id: 440386
ClinVar RCV Id: RCV001618721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061950.2:p.Asn129Lys
CA2178266
NM_019077.3:c.387T>G
CA351085476
NM_019077.3:c.387T>A