Allele Registry

Canonical Allele Identifier: PA915984528

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007984

RCV000486508

ClinVar Variation:

7548

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139328.1:p.Pro475Arg	CA254207 NM_001145856.2:c.1424C>G