Canonical Allele Identifier: PA2827790047
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 450573
ClinVar RCV Id: RCV000519145 RCV001497480
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Gln1908Glu
CA349063734
NM_001353960.2:c.5722C>G