Canonical Allele Identifier: PA2573232413
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353929
ClinVar RCV Id: RCV001863673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Asn87Thr
CA365948862
NM_003764.4:c.260A>C