Canonical Allele Identifier: PA645430059
Gene: STX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 355600
ClinVar RCV Id: RCV000320630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003755.2:p.Phe72Leu
CA4031654
NM_003764.4:c.214T>C
CA365948770
NM_003764.4:c.216C>A
CA365948771
NM_003764.4:c.216C>G