Canonical Allele Identifier: PA2828476374
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1074301
ClinVar RCV Id: RCV001387541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Ile1596Ser
CA349036859
NM_001371247.1:c.4787T>G