Canonical Allele Identifier: PA915986743
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 801814
ClinVar RCV Id: RCV000986907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Asn359Lys
CA349071316
NM_006920.6:c.1077T>G
CA349071317
NM_006920.6:c.1077T>A