Allele Registry

Canonical Allele Identifier: PA916030639

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224757

ClinVar Variation:

235833

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337680.1:p.Val977Ala	CA10581444 NM_001350751.2:c.2930T>C