Allele Registry

Canonical Allele Identifier: PA2826243840

Gene: NCR2 HGNC NCBI

ClinVar Allele:

2279410

ClinVar RCV:

RCV004141956

ClinVar Variation:

2290904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186438.1:p.Gly267Ala	CA364068239 NM_001199509.2:c.800G>C