Canonical Allele Identifier: PA2741906059
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2805143
ClinVar RCV Id: RCV003613545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Arg96Trp
CA365948919
NM_003764.4:c.286C>T