Canonical Allele Identifier: PA2573232420
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1425938
ClinVar RCV Id: RCV001927019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Gly97Arg
CA365948924
NM_003764.4:c.289G>C