Allele Registry

Canonical Allele Identifier: PA2827569978

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000408614

ClinVar Variation:

369675

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337680.1:p.Arg329Gly	CA10654765 NM_001350751.2:c.985A>G