Allele Registry

Canonical Allele Identifier: PA645495476

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224242

ClinVar Variation:

235835

HGVS (amino-acid)	Matching Registered Transcripts
NP_443099.1:p.Phe512Val	CA10581446 NM_052867.4:c.1534T>G