Allele Registry

Canonical Allele Identifier: PA915984519

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007986

ClinVar Variation:

7550

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139328.1:p.Arg472Pro	CA254209 NM_001145856.2:c.1415G>C