Canonical Allele Identifier: PA2580336328
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 2499708
ClinVar RCV Id: RCV003223800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008853.3:p.Ala1327Pro
CA349026065
NM_006922.4:c.3979G>C