Canonical Allele Identifier: PA2827774616
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Val1619Met
CA284988
NM_001353952.2:c.4855G>A