Canonical Allele Identifier: PA2827786199
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2015187
ClinVar RCV Id: RCV002839333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Phe1403Leu
CA349049627
NM_001353958.2:c.4209C>A
CA349049628
NM_001353958.2:c.4209C>G
CA349049633
NM_001353958.2:c.4207T>C