Allele Registry

Canonical Allele Identifier: PA2827568570

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000167530

ClinVar Variation:

187773

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337677.1:p.Leu590Phe	CA198512 NM_001350748.2:c.1768C>T