Canonical Allele Identifier: PA2827569721
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1699650
ClinVar RCV Id: RCV002273507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337679.1:p.Trp1240Arg
CA7035290
NM_001350750.2:c.3718T>C
CA388650384
NM_001350750.2:c.3718T>A