Canonical Allele Identifier: PA2827756783
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190017
ClinVar RCV Id: RCV000180973 RCV003228910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ala342Ser
CA303563
NM_001353949.2:c.1024G>T