Canonical Allele Identifier: PA2826012647
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68607
ClinVar RCV Id: RCV000059484 RCV001387943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Cys931Arg
CA285105
NM_001165964.3:c.2791T>C