Canonical Allele Identifier: PA214588
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 194857
ClinVar RCV Id: RCV000175322 RCV000857921 RCV002492743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008853.3:p.Val1084Ile
CA214587
NM_006922.4:c.3250G>A