Canonical Allele Identifier: PA1139705273
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 838955
ClinVar RCV Id: RCV001040614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Gly97Ser
CA365948923
NM_003764.4:c.289G>A