Canonical Allele Identifier: PA2826260139
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1067239
ClinVar RCV Id: RCV001378447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ile1545Lys
CA349072268
NM_001202435.3:c.4634T>A