Canonical Allele Identifier: PA2827569390
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2525647
ClinVar RCV Id: RCV003279822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337679.1:p.Val273Ile
CA256071329
NM_001350750.2:c.817G>A