Canonical Allele Identifier: PA2826008922
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2720425
ClinVar RCV Id: RCV003590813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Thr184Ala
CA1943491
NM_001165963.4:c.550A>G