Canonical Allele Identifier: PA913195669
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 593872
ClinVar RCV Id: RCV000729035 RCV001058607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Asp45Gly
CA349243095
NM_006920.6:c.134A>G