Allele Registry

Canonical Allele Identifier: PA2827569122

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000167764

RCV000224736

RCV001267339

RCV001390781

ClinVar Variation:

188046

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Arg1181Gln	CA212642 NM_001350749.2:c.3542G>A