Canonical Allele Identifier: PA2580229743
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2002938
ClinVar RCV Id: RCV002833103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Leu495Pro
CA349053255
NM_001353961.2:c.1484T>C