Allele Registry

Canonical Allele Identifier: PA2826243838

Gene: NCR2 HGNC NCBI

ClinVar RCV:

RCV004131229

ClinVar Variation:

2278176

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186438.1:p.Ala162Asp	CA364066068 NM_001199509.2:c.485C>A