Canonical Allele Identifier: PA2827786835
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2762703
ClinVar RCV Id: RCV003590314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Val1756Leu
CA349068046
NM_001353958.2:c.5266G>C