Canonical Allele Identifier: PA2827775802
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 429575
ClinVar RCV Id: RCV000492923 RCV001390613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Thr363Pro
CA349071283
NM_001353954.2:c.1087A>C