Allele Registry

Canonical Allele Identifier: PA645510262

Gene: UGT1A7 HGNC NCBI

ClinVar RCV:

RCV001618721

ClinVar Variation:

440386

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