Allele Registry

Canonical Allele Identifier: PA2580312150

Gene: NCR2 HGNC NCBI

ClinVar Allele:

2279410

ClinVar RCV:

RCV004141956

ClinVar Variation:

2290904

HGVS (amino-acid)	Matching Registered Transcripts
NP_004819.2:p.Trp219Cys	CA364068239 NM_004828.4:c.657G>C CA364068240 NM_004828.4:c.657G>T