Allele Registry

Canonical Allele Identifier: PA2827569482

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000167532

RCV000483507

ClinVar Variation:

187775

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337679.1:p.Tyr549Ser	CA198516 NM_001350750.2:c.1646A>C