Canonical Allele Identifier: PA2580296019
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1962494
ClinVar RCV Id: RCV002735119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Glu31Lys
CA4031617
NM_003764.4:c.91G>A