Allele Registry

Canonical Allele Identifier: PA2827570057

Gene: NALCN HGNC NCBI

ClinVar RCV:

RCV000486031

ClinVar Variation:

421882

HGVS (amino-acid)	Matching Registered Transcripts
NP_001337680.1:p.Ser563Arg	CA16619608 NM_001350751.2:c.1689T>G CA388702937 NM_001350751.2:c.1689T>A CA388702943 NM_001350751.2:c.1687A>C