Canonical Allele Identifier: PA2827753531
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Tyr1422Cys
CA284949
NM_001353948.2:c.4265A>G