Canonical Allele Identifier: PA2825399267
Gene: UGT2B15 HGNC NCBI

Linked Data

ClinVar Variation Id: 3186198
ClinVar RCV Id: RCV004479596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001067.2:p.Gln205His
CA2942671
NM_001076.4:c.615A>C
CA357085092
NM_001076.4:c.615A>T