Allele Registry

Canonical Allele Identifier: PA2825341602

Gene: NQO1 HGNC NCBI

ClinVar Allele:

31848

ClinVar RCV:

RCV000018300

RCV000018301

RCV000018302

RCV000434090

RCV003974839

ClinVar Variation:

16809

HGVS (amino-acid)	Matching Registered Transcripts
NP_001020604.1:p.Pro153Ser	CA126904 NM_001025433.2:c.457C>T