Allele Registry

Canonical Allele Identifier: PA2827569452

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000167531

ClinVar Variation:

187774

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337679.1:p.Leu480Ser	CA198514 NM_001350750.2:c.1439T>C