Allele Registry

Canonical Allele Identifier: PA913201408

Gene: SH3BP2 HGNC NCBI

ClinVar Allele:

264193

ClinVar RCV:

RCV000293867

RCV001261155

ClinVar Variation:

280675

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139327.1:p.Pro446Ser	CA10602925 NM_001145855.2:c.1336C>T