Allele Registry

Canonical Allele Identifier: PA2827570021

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224900

ClinVar Variation:

235834

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337680.1:p.Thr484Asn	CA10581445 NM_001350751.2:c.1451C>A