Canonical Allele Identifier: PA2827569690
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 188046
ClinVar RCV Id: RCV000167764 RCV000224736 RCV001267339 RCV001390781
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337679.1:p.Arg1152Gln
CA212642
NM_001350750.2:c.3455G>A