Canonical Allele Identifier: PA284951
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68540
ClinVar RCV Id: RCV000059414 RCV001048734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Tyr1411Cys
CA284949
NM_006920.6:c.4232A>G