Canonical Allele Identifier: PA916051247
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 784273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443099.1:p.Arg295Cys
CA7036362
NM_052867.4:c.883C>T