Allele Registry

Canonical Allele Identifier: PA2827569205

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224385

ClinVar Variation:

235830

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Ile1446Met	CA10581441 NM_001350749.2:c.4338T>G