Canonical Allele Identifier: PA2827777027
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1016678
ClinVar RCV Id: RCV001315714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Cys1273Tyr
CA349053965
NM_001353954.2:c.3818G>A