Canonical Allele Identifier: PA2827774759
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801500
ClinVar RCV Id: RCV003223438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Glu1687Gly
CA349069248
NM_001353952.2:c.5060A>G