Allele Registry

Canonical Allele Identifier: PA198517

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000167532

RCV000483507

ClinVar Variation:

187775

HGVS (amino-acid)	Matching Registered Transcripts
NP_443099.1:p.Tyr578Ser	CA198516 NM_052867.4:c.1733A>C