Canonical Allele Identifier: PA2826946635
Gene: NFE2L2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300833.1:p.Arg3Gly
CA349380477
NM_001313904.1:c.7A>G