Canonical Allele Identifier: PA916030642
Gene: NALCN HGNC NCBI

Linked Data

ClinVar Variation Id: 520429
ClinVar RCV Id: RCV000622774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337680.1:p.Ile993Val
CA388654881
NM_001350751.2:c.2977A>G