Canonical Allele Identifier: PA2827757488
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1045626
ClinVar RCV Id: RCV001350071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.His553Tyr
CA349068240
NM_001353949.2:c.1657C>T