Canonical Allele Identifier: PA2829675600
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1490559
ClinVar RCV Id: RCV002001790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Val1158Gly
CA349056679
NM_006920.6:c.3473T>G