Canonical Allele Identifier: PA2828476354
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 464912
ClinVar RCV Id: RCV000548002 RCV000857242 RCV002319532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Tyr1589Cys
CA349036779
NM_001371247.1:c.4766A>G