Allele Registry

Canonical Allele Identifier: PA915984531

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007985

ClinVar Variation:

7549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139328.1:p.Pro475His	CA254208 NM_001145856.2:c.1424C>A CA2586973589 NM_001145856.2:c.1424_1425delinsAT