Canonical Allele Identifier: PA2826014277
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1210876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Lys1979Glu
CA59797669
NM_001165964.3:c.5935A>G