Canonical Allele Identifier: PA2827789901
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2443596
ClinVar RCV Id: RCV003152203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Pro1813Leu
CA349065614
NM_001353960.2:c.5438C>T