Allele Registry

Canonical Allele Identifier: PA2827568654

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224534

ClinVar Variation:

235832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337677.1:p.Ile1046Thr	CA10581443 NM_001350748.2:c.3137T>C