Canonical Allele Identifier: PA2827568818
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1176328
ClinVar RCV Id: RCV001531806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337678.1:p.Ala277Ser
CA7036366
NM_001350749.2:c.829G>T