Canonical Allele Identifier: PA915984459
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348584
ClinVar RCV Id: RCV000400486 RCV002520236
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139328.1:p.Val438Met
CA2819397
NM_001145856.2:c.1312G>A