Canonical Allele Identifier: PA317964
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 206999
ClinVar RCV Id: RCV000189150 RCV001265491 RCV003325951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Lys1422Glu
CA317963
NM_021007.3:c.4264A>G