Canonical Allele Identifier: PA2829675665
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 461265
ClinVar RCV Id: RCV000540121

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Trp1208Arg
CA349055964
NM_006920.6:c.3622T>C
CA349055968
NM_006920.6:c.3622T>A