Canonical Allele Identifier: PA2828476321
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 12877
ClinVar RCV Id: RCV000013737 RCV002319421 RCV002513022 RCV000255820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Leu1563Val
CA122769
NM_001371247.1:c.4687C>G