Canonical Allele Identifier: PA2827787302
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 423370
ClinVar RCV Id: RCV000481610 RCV001262228 RCV001851250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Leu117Pro
CA16617318
NM_001353960.2:c.350T>C