Allele Registry

Canonical Allele Identifier: PA645510264

Gene: UGT1A7 HGNC NCBI

ClinVar RCV:

RCV001692163

ClinVar Variation:

440389

HGVS (amino-acid)	Matching Registered Transcripts
NP_061950.2:p.Trp208Arg	CA2178317 NM_019077.3:c.622T>C CA351087625 NM_019077.3:c.622T>A