Canonical Allele Identifier: PA2827780869
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 265303
ClinVar RCV Id: RCV000255765 RCV000624688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Tyr1757Cys
CA10588317
NM_001353955.2:c.5270A>G