Canonical Allele Identifier: PA2827568821
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 872450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337678.1:p.Arg295His
CA7036361
NM_001350749.2:c.884G>A