Allele Registry

Canonical Allele Identifier: PA645492567

Gene: NFE2L2 HGNC NCBI

ClinVar RCV:

RCV000424276

RCV000427125

RCV000432126

RCV000434556

RCV000442314

RCV000442352

RCV000445333

ClinVar Variation:

376461

HGVS (amino-acid)	Matching Registered Transcripts
NP_006155.2:p.Asp29His	CA16602895 NM_006164.5:c.85G>C