Canonical Allele Identifier: PA2826258022
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2848612
ClinVar RCV Id: RCV003754682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Thr105Ser
CA349077082
NM_001202435.3:c.314C>G
CA349077084
NM_001202435.3:c.313A>T