Canonical Allele Identifier: PA2826012360
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 856834
ClinVar RCV Id: RCV001062381
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Thr754Ser
CA349064124
NM_001165964.3:c.2261C>G
CA349064129
NM_001165964.3:c.2260A>T