Canonical Allele Identifier: PA2827569959
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1921742
ClinVar RCV Id: RCV002613261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337680.1:p.Glu275Lys
CA388705148
NM_001350751.2:c.823G>A