Canonical Allele Identifier: PA2741866799
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2707845
ClinVar RCV Id: RCV003589893
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Leu861Phe
CA349069648
NM_001353961.2:c.2581C>T