Allele Registry

Canonical Allele Identifier: PA2825891461

Gene: NFE2L2 HGNC NCBI

ClinVar RCV:

RCV000421608

RCV000425359

RCV000426059

RCV000431763

RCV000432841

RCV000441859

RCV000441968

ClinVar Variation:

376464

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138884.1:p.Asp13Gly	CA16602898 NM_001145412.3:c.38A>G