Canonical Allele Identifier: PA2830141140
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_443099.1:p.Val1285Ile
CA7035277
NM_052867.4:c.3853G>A