Canonical Allele Identifier: PA2827569392
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1921742
ClinVar RCV Id: RCV002613261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337679.1:p.Glu275Lys
CA388705148
NM_001350750.2:c.823G>A