Allele Registry

Canonical Allele Identifier: PA915984382

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000320509

ClinVar Variation:

348576

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139328.1:p.Pro223Leu	CA2819192 NM_001145856.2:c.668C>T