Canonical Allele Identifier: PA2827766711
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 372903
ClinVar RCV Id: RCV000414265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Gln1416Leu
CA16042437
NM_001353950.2:c.4247A>T