Allele Registry

Canonical Allele Identifier: PA2825585889

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000293867

RCV001261155

ClinVar Variation:

280675

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116153.1:p.Pro418Ser	CA10602925 NM_001122681.1:c.1252C>T