Allele Registry

Canonical Allele Identifier: PA2827570020

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224242

ClinVar Variation:

235835

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337680.1:p.Phe483Val	CA10581446 NM_001350751.2:c.1447T>G