Canonical Allele Identifier: PA2827753030
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 662021
ClinVar RCV Id: RCV000819559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Val1297Gly
CA1942867
NM_001353948.2:c.3890T>G