Allele Registry

Canonical Allele Identifier: PA2827569933

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000167528

ClinVar Variation:

187771

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337680.1:p.Gln177Pro	CA198508 NM_001350751.2:c.530A>C