Canonical Allele Identifier: PA318026
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 932954
ClinVar RCV Id: RCV001200928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Gly1634Asp
CA318024
NM_021007.3:c.4901G>A