Canonical Allele Identifier: PA2827783604
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206854
ClinVar RCV Id: RCV000188988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Arg1620Leu
CA317561
NM_001353957.2:c.4859G>T