Canonical Allele Identifier: PA2825353690
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2939257
ClinVar RCV Id: RCV003791983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Ala263Gly
CA349018095
NM_001040142.2:c.788C>G