Canonical Allele Identifier: PA318121
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207056
ClinVar RCV Id: RCV000189210 RCV001379442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Glu430Gly
CA318120
NM_001040142.2:c.1289A>G