Canonical Allele Identifier: PA2827786366
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Pro1491Thr
CA317497
NM_001353958.2:c.4471C>A