Allele Registry

Canonical Allele Identifier: PA645495491

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224534

ClinVar Variation:

235832

HGVS (amino-acid)	Matching Registered Transcripts
NP_443099.1:p.Ile1017Thr	CA10581443 NM_052867.4:c.3050T>C