Canonical Allele Identifier: PA2580296024
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2056496
ClinVar RCV Id: RCV002947513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Arg64Gln
CA365948719
NM_003764.4:c.191G>A