Canonical Allele Identifier: PA2827780992
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Pro1825Leu
CA317617
NM_001353955.2:c.5474C>T