Canonical Allele Identifier: PA2827777029
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Leu1275Pro
CA285150
NM_001353954.2:c.3824T>C