Canonical Allele Identifier: PA2827786651
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2752271
ClinVar RCV Id: RCV003589992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Ser1662Pro
CA349069400
NM_001353958.2:c.4984T>C