Allele Registry

Canonical Allele Identifier: PA913201412

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007989

ClinVar Variation:

7553

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139327.1:p.Gly448Glu	CA254212 NM_001145855.2:c.1343G>A