Allele Registry

Canonical Allele Identifier: PA2827568885

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000167531

ClinVar Variation:

187774

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337678.1:p.Leu509Ser	CA198514 NM_001350749.2:c.1526T>C