Canonical Allele Identifier: PA645495476
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 235835
ClinVar RCV Id: RCV000224242
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443099.1:p.Phe512Val
CA10581446
NM_052867.4:c.1534T>G