Allele Registry

Canonical Allele Identifier: PA2580312148

Gene: NCR2 HGNC NCBI

ClinVar RCV:

RCV004131229

ClinVar Variation:

2278176

HGVS (amino-acid)	Matching Registered Transcripts
NP_004819.2:p.Ala162Asp	CA364066068 NM_004828.4:c.485C>A