Canonical Allele Identifier: PA1139697883
Gene: STXBP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 969042
ClinVar RCV Id: RCV001244298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258963.1:p.Gly552Cys
CA403162082
NM_001272034.2:c.1654G>T