Canonical Allele Identifier: PA2829676759
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 498246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Lys1985Asn
CA59797683
NM_006920.6:c.5955A>C
CA349063033
NM_006920.6:c.5955A>T