Canonical Allele Identifier: PA2827774566
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Arg1585Cys
CA145250
NM_001353952.2:c.4753C>T