Allele Registry

Canonical Allele Identifier: PA645492578

Gene: NFE2L2 HGNC NCBI

ClinVar Allele:

363347

ClinVar RCV:

RCV000426287

RCV000427358

RCV000437586

RCV000438261

RCV000442131

RCV000445098

ClinVar Variation:

376468

HGVS (amino-acid)	Matching Registered Transcripts
NP_006155.2:p.Glu79Asp	CA16602902 NM_006164.5:c.237G>T CA349380470 NM_006164.5:c.237G>C