Canonical Allele Identifier: PA2827569453
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 235835
ClinVar RCV Id: RCV000224242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337679.1:p.Phe483Val
CA10581446
NM_001350750.2:c.1447T>G