Canonical Allele Identifier: PA2827569634
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 520429
ClinVar RCV Id: RCV000622774
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337679.1:p.Ile993Val
CA388654881
NM_001350750.2:c.2977A>G