Canonical Allele Identifier: PA2827775800
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2099693
ClinVar RCV Id: RCV003021836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Tyr362Cys
CA349071288
NM_001353954.2:c.1085A>G