Allele Registry

Canonical Allele Identifier: PA2827569058

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224757

ClinVar Variation:

235833

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Val1006Ala	CA10581444 NM_001350749.2:c.3017T>C