Allele Registry

Canonical Allele Identifier: PA645492572

Gene: NFE2L2 HGNC NCBI

ClinVar RCV:

RCV000418369

RCV000419012

RCV000424664

RCV000425738

RCV000430352

RCV000434952

RCV000436001

ClinVar Variation:

376462

HGVS (amino-acid)	Matching Registered Transcripts
NP_006155.2:p.Asp29Tyr	CA16602896 NM_006164.5:c.85G>T