Canonical Allele Identifier: PA2827769818
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 801814
ClinVar RCV Id: RCV000986907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Asn359Lys
CA349071316
NM_001353951.2:c.1077T>G
CA349071317
NM_001353951.2:c.1077T>A