Canonical Allele Identifier: PA2827568482
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 985383
ClinVar RCV Id: RCV001266253
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337677.1:p.Arg329Thr
CA388704761
NM_001350748.2:c.986G>C