Allele Registry

Canonical Allele Identifier: PA2825891459

Gene: NFE2L2 HGNC NCBI

ClinVar RCV:

RCV000424276

RCV000427125

RCV000432126

RCV000434556

RCV000442314

RCV000442352

RCV000445333

ClinVar Variation:

376461

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138884.1:p.Asp13His	CA16602895 NM_001145412.3:c.37G>C