Canonical Allele Identifier: PA2825353906
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2939619
ClinVar RCV Id: RCV003794785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Leu389Val
CA1939762
NM_001040142.2:c.1165C>G