Allele Registry

Canonical Allele Identifier: PA2827569683

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224193

ClinVar Variation:

235831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337679.1:p.Thr1136Pro	CA10581442 NM_001350750.2:c.3406A>C