Canonical Allele Identifier: PA2828476348
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 839176
ClinVar RCV Id: RCV001040872 RCV003320791 RCV003396641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Val1579Ala
CA349036680
NM_001371247.1:c.4736T>C