Allele Registry

Canonical Allele Identifier: PA916030641

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224534

ClinVar Variation:

235832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337680.1:p.Ile988Thr	CA10581443 NM_001350751.2:c.2963T>C