Allele Registry

Canonical Allele Identifier: PA915984371

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000261336

ClinVar Variation:

348572

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139328.1:p.Ser204Leu	CA2819177 NM_001145856.2:c.611C>T