Canonical Allele Identifier: PA2827787094
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_001340887.1:p.Asn1924Ile
CA349063514
NM_001353958.2:c.5771A>T