Allele Registry

Canonical Allele Identifier: PA126905

Gene: NQO1 HGNC NCBI

ClinVar RCV:

RCV000018300

RCV000018301

RCV000018302

RCV000434090

RCV003974839

ClinVar Variation:

16809

HGVS (amino-acid)	Matching Registered Transcripts
NP_000894.1:p.Pro187Ser	CA126904 NM_000903.3:c.559C>T