Allele Registry

Canonical Allele Identifier: PA2827569116

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224193

ClinVar Variation:

235831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Thr1165Pro	CA10581442 NM_001350749.2:c.3493A>C