Canonical Allele Identifier: PA916005516
Gene: STXBP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258963.1:p.Gly552Ser
CA260033
NM_001272034.2:c.1654G>A