Allele Registry

Canonical Allele Identifier: PA2827568650

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224757

ClinVar Variation:

235833

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337677.1:p.Val1035Ala	CA10581444 NM_001350748.2:c.3104T>C