Canonical Allele Identifier: PA2827781832
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1013695
ClinVar RCV Id: RCV001312320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Thr391Ser
CA349071050
NM_001353957.2:c.1171A>T