Allele Registry

Canonical Allele Identifier: PA915984540

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007989

ClinVar Variation:

7553

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139328.1:p.Gly477Glu	CA254212 NM_001145856.2:c.1430G>A