Canonical Allele Identifier: PA2827775228
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 498246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Lys1985Asn
CA59797683
NM_001353952.2:c.5955A>C
CA349063033
NM_001353952.2:c.5955A>T