Canonical Allele Identifier: PA239348
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 193734
ClinVar RCV Id: RCV000364025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Thr393Lys
CA239346
NM_021007.3:c.1178C>A