Allele Registry

Canonical Allele Identifier: PA645495497

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224385

ClinVar Variation:

235830

HGVS (amino-acid)	Matching Registered Transcripts
NP_443099.1:p.Ile1446Met	CA10581441 NM_052867.4:c.4338T>G