Canonical Allele Identifier: PA2827762127
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2061979
ClinVar RCV Id: RCV002923463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Asn1941Ile
CA349063514
NM_001353949.2:c.5822A>T