Canonical Allele Identifier: PA891851628
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 576251
ClinVar RCV Id: RCV000698709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Lys94Arg
CA4031669
NM_003764.4:c.281A>G