Canonical Allele Identifier: PA303570
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190018
ClinVar RCV Id: RCV000180974 RCV003588585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Tyr349Cys
CA303567
NM_006920.6:c.1046A>G