Canonical Allele Identifier: PA2827783770
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 834858
ClinVar RCV Id: RCV001035628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Asp1699Tyr
CA349068756
NM_001353957.2:c.5095G>T