Allele Registry

Canonical Allele Identifier: PA645495477

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000224900

ClinVar Variation:

235834

HGVS (amino-acid)	Matching Registered Transcripts
NP_443099.1:p.Thr513Asn	CA10581445 NM_052867.4:c.1538C>A