Canonical Allele Identifier: PA2825353278
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1028208
ClinVar RCV Id: RCV001329198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Ile123Leu
CA349011918
NM_001040142.2:c.367A>C