Canonical Allele Identifier: PA2573232415
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1496752
ClinVar RCV Id: RCV001992036
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Ala90_Ala92del
CA2573140694
NM_003764.4:c.268_276del