Canonical Allele Identifier: PA2827569452
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 187774
ClinVar RCV Id: RCV000167531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337679.1:p.Leu480Ser
CA198514
NM_001350750.2:c.1439T>C