Canonical Allele Identifier: PA2828473875
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1690637
ClinVar RCV Id: RCV002253055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Ala215Glu
CA349017437
NM_001371247.1:c.644C>A