Canonical Allele Identifier: PA2827788556
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 449377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Asp977Glu
CA1943019
NM_001353960.2:c.2931T>G
CA349060373
NM_001353960.2:c.2931T>A