Allele Registry

Canonical Allele Identifier: PA2825921094

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV002052435

ClinVar Variation:

1526420

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139327.1:p.Gly448Ala	CA356057584 NM_001145855.2:c.1343G>C