Canonical Allele Identifier: PA2827778792
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 499554
ClinVar RCV Id: RCV000597440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Ser364Ile
CA349071270
NM_001353955.2:c.1091G>T