Allele Registry

Canonical Allele Identifier: PA913201406

Gene: SH3BP2 HGNC NCBI

ClinVar Allele:

22590

ClinVar RCV:

RCV000007987

RCV003886359

ClinVar Variation:

7551

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139327.1:p.Arg443Gln	CA254210 NM_001145855.2:c.1328G>A