Allele Registry

Canonical Allele Identifier: PA2827569772

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224385

ClinVar Variation:

235830

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337679.1:p.Ile1417Met	CA10581441 NM_001350750.2:c.4251T>G