Canonical Allele Identifier: PA2827760966
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Arg1637Cys
CA285189
NM_001353949.2:c.4909C>T