Canonical Allele Identifier: PA2827783000
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2704798
ClinVar RCV Id: RCV003589804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Ser1267Ala
CA349053533
NM_001353957.2:c.3799T>G