Canonical Allele Identifier: PA2826014213
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1715838
ClinVar RCV Id: RCV002304639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Phe1912Tyr
CA349063678
NM_001165964.3:c.5735T>A