Allele Registry

Canonical Allele Identifier: PA915984578

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000269056

ClinVar Variation:

348593

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139328.1:p.Ser562Cys	CA2819599 NM_001145856.2:c.1685C>G