Canonical Allele Identifier: PA2827773954
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2086222
ClinVar RCV Id: RCV003007379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Ser1221Arg
CA349055656
NM_001353952.2:c.3663T>G
CA349055659
NM_001353952.2:c.3663T>A
CA349055672
NM_001353952.2:c.3661A>C