Allele Registry

Canonical Allele Identifier: PA916030635

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224385

ClinVar Variation:

235830

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337677.1:p.Ile1475Met	CA10581441 NM_001350748.2:c.4425T>G