Canonical Allele Identifier: PA2826011711
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1418113
ClinVar RCV Id: RCV001951947 RCV002479417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Gly271Ser
CA349073228
NM_001165964.3:c.811G>A