Canonical Allele Identifier: PA2826259512
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 521780
ClinVar RCV Id: RCV000624256 RCV001543134 RCV002510935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Pro1177Arg
CA1942938
NM_001202435.3:c.3530C>G