Canonical Allele Identifier: PA2827756286
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 662029
ClinVar RCV Id: RCV000819574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ala214Thr
CA349074256
NM_001353949.2:c.640G>A