Canonical Allele Identifier: PA2826259724
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 69407
ClinVar RCV Id: RCV001304935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Lys1313Gln
CA59772659
NM_001202435.3:c.3937A>C