Canonical Allele Identifier: PA303596
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190028
ClinVar RCV Id: RCV000180984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Tyr1263Ser
CA303594
NM_006920.6:c.3788A>C