Allele Registry

Canonical Allele Identifier: PA2827569970

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000167529

ClinVar Variation:

187772

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337680.1:p.Val313Gly	CA198510 NM_001350751.2:c.938T>G