Allele Registry

Canonical Allele Identifier: PA101334

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007989

ClinVar Variation:

7553

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116153.1:p.Gly420Glu	CA254212 NM_001122681.1:c.1259G>A