Canonical Allele Identifier: PA2827569161
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1301424
ClinVar RCV Id: RCV001733434 RCV003298958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337678.1:p.Val1285Ile
CA7035277
NM_001350749.2:c.3853G>A