Canonical Allele Identifier: PA2827785455
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Arg903Cys
CA273369
NM_001353958.2:c.2707C>T