Canonical Allele Identifier: PA2827776481
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Leu885Ser
CA303322
NM_001353954.2:c.2654T>C