Canonical Allele Identifier: PA2827778862
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2734312
ClinVar RCV Id: RCV003588467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Gly396Glu
CA349071023
NM_001353955.2:c.1187G>A