Canonical Allele Identifier: PA2827772788
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Tyr349Cys
CA303567
NM_001353952.2:c.1046A>G