Canonical Allele Identifier: PA317555
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206852
ClinVar RCV Id: RCV000188984 RCV001244268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Arg1628Pro
CA317553
NM_006920.6:c.4883G>C