Allele Registry

Canonical Allele Identifier: PA913201390

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000265353

RCV002520235

ClinVar Variation:

348575

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139327.1:p.Arg186Trp	CA2819186 NM_001145855.2:c.556C>T