Allele Registry

Canonical Allele Identifier: PA101325

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007988

RCV000414728

RCV002523913

ClinVar Variation:

7552

372503

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116153.1:p.Gly420Arg	CA254211 NM_001122681.1:c.1258G>C CA16042561 NM_001122681.1:c.1258G>A