Allele Registry

Canonical Allele Identifier: PA2827569062

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224534

ClinVar Variation:

235832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Ile1017Thr	CA10581443 NM_001350749.2:c.3050T>C