Allele Registry

Canonical Allele Identifier: PA645495485

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000486031

ClinVar Variation:

421882

HGVS (amino-acid)	Matching Registered Transcripts
NP_443099.1:p.Ser592Arg	CA16619608 NM_052867.4:c.1776T>G CA388702937 NM_052867.4:c.1776T>A CA388702943 NM_052867.4:c.1774A>C