Canonical Allele Identifier: PA2829676710
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 450573
ClinVar RCV Id: RCV000519145 RCV001497480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Gln1926Glu
CA349063734
NM_006920.6:c.5776C>G