Allele Registry

Canonical Allele Identifier: PA2827569483

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000498669

RCV001254037

ClinVar Variation:

254646

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337679.1:p.Tyr549Cys	CA388703427 NM_001350750.2:c.1646A>G