Canonical Allele Identifier: PA2826012375
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Tyr762Cys
CA266101
NM_001165964.3:c.2285A>G