Canonical Allele Identifier: PA106931
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68543
ClinVar RCV Id: RCV000059417 RCV001267274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala1441Pro
CA284958
NM_001165963.4:c.4321G>C