Canonical Allele Identifier: PA2829674907
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2435670
ClinVar RCV Id: RCV003142757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Glu714Asp
CA349065533
NM_006920.6:c.2142A>T
CA349065536
NM_006920.6:c.2142A>C