Allele Registry

Canonical Allele Identifier: PA2827569408

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224921

ClinVar Variation:

235836

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337679.1:p.Glu327Lys	CA10581447 NM_001350750.2:c.979G>A