Allele Registry

Canonical Allele Identifier: PA913201405

Gene: SH3BP2 HGNC NCBI

ClinVar Allele:

22589

ClinVar RCV:

RCV000007986

ClinVar Variation:

7550

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139327.1:p.Arg443Pro	CA254209 NM_001145855.2:c.1328G>C