Canonical Allele Identifier: PA2826135001
Gene: STX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1390887
ClinVar RCV Id: RCV001910858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171511.1:p.Arg125Trp
CA6020865
NM_001178040.1:c.373C>T