Canonical Allele Identifier: PA2827773945
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 976067
ClinVar RCV Id: RCV001253246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Leu1218Pro
CA349055713
NM_001353952.2:c.3653T>C