Canonical Allele Identifier: PA2827569396
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 784273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337679.1:p.Arg295Cys
CA7036362
NM_001350750.2:c.883C>T