Canonical Allele Identifier: PA2827770960
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68618
ClinVar RCV Id: RCV000059495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ser1220Thr
CA285132
NM_001353951.2:c.3659G>C