Canonical Allele Identifier: PA2828472138
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2169503
ClinVar RCV Id: RCV003093180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Ile1252Val
CA1940171
NM_001371246.1:c.3754A>G