Canonical Allele Identifier: PA2827786860
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1034883
ClinVar RCV Id: RCV001337672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Pro1771His
CA349067802
NM_001353958.2:c.5312C>A