Canonical Allele Identifier: PA2827767462
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68557
ClinVar RCV Id: RCV000059431 RCV000176634 RCV000463147 RCV000623263 RCV002281560 RCV003448258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Arg1625Gln
CA145253
NM_001353950.2:c.4874G>A