Allele Registry

Canonical Allele Identifier: PA2827569489

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000167530

ClinVar Variation:

187773

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337679.1:p.Leu561Phe	CA198512 NM_001350750.2:c.1681C>T