Canonical Allele Identifier: PA234875
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Arg542Gln
CA234872
NM_006920.6:c.1625G>A