Allele Registry

Canonical Allele Identifier: PA916030624

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224193

ClinVar Variation:

235831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337677.1:p.Thr1194Pro	CA10581442 NM_001350748.2:c.3580A>C