Canonical Allele Identifier: PA1139705294
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 845351
ClinVar RCV Id: RCV001048397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Glu98Lys
CA365948930
NM_003764.4:c.292G>A