Canonical Allele Identifier: PA2827568659
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_001337677.1:p.Ile1051Val
CA388654881
NM_001350748.2:c.3151A>G