Canonical Allele Identifier: PA2826258961
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 856834
ClinVar RCV Id: RCV001062381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Thr782Ser
CA349064124
NM_001202435.3:c.2345C>G
CA349064129
NM_001202435.3:c.2344A>T