Canonical Allele Identifier: PA204868
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 208771
ClinVar RCV Id: RCV000190794 RCV001133331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Phe1213Val
CA204867
NM_001040142.2:c.3637T>G