Canonical Allele Identifier: PA2827774090
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 663255
ClinVar RCV Id: RCV000821102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Arg1308Gly
CA349053101
NM_001353952.2:c.3922A>G