Allele Registry

Canonical Allele Identifier: PA2827568887

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224900

ClinVar Variation:

235834

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Thr513Asn	CA10581445 NM_001350749.2:c.1538C>A