Allele Registry

Canonical Allele Identifier: PA2827568916

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000498669

RCV001254037

ClinVar Variation:

254646

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Tyr578Cys	CA388703427 NM_001350749.2:c.1733A>G