Canonical Allele Identifier: PA2826013002
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68532
ClinVar RCV Id: RCV000059405 RCV000723903 RCV001476333 RCV001836728
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Glu1210Asp
CA234849
NM_001165964.3:c.3630A>C
CA349054671
NM_001165964.3:c.3630A>T