Canonical Allele Identifier: PA2741933686
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 2689913
ClinVar RCV Id: RCV003491434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008853.3:p.Ser1376Thr
CA349025529
NM_006922.4:c.4127G>C