Allele Registry

Canonical Allele Identifier: PA2825891697

Gene: NFE2L2 HGNC NCBI

ClinVar RCV:

RCV000419375

RCV000423965

RCV000429636

RCV000434234

RCV000440548

RCV000441021

RCV000441645

ClinVar Variation:

376463

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138885.1:p.Asp13Asn	CA16602897 NM_001145413.3:c.37G>A