Canonical Allele Identifier: PA2827789849
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1438229
ClinVar RCV Id: RCV001934229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Glu1781Lys
CA349067630
NM_001353960.2:c.5341G>A