Allele Registry

Canonical Allele Identifier: PA2827568886

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224242

ClinVar Variation:

235835

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Phe512Val	CA10581446 NM_001350749.2:c.1534T>G