Canonical Allele Identifier: PA916036933
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189845
ClinVar RCV Id: RCV000180799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Pro854Arg
CA303095
NM_001353961.2:c.2561C>G