Canonical Allele Identifier: PA2827774458
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Pro1508Leu
CA317501
NM_001353952.2:c.4523C>T