Allele Registry

Canonical Allele Identifier: PA913201410

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007985

ClinVar Variation:

7549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139327.1:p.Pro446His	CA254208 NM_001145855.2:c.1337C>A CA2586973589 NM_001145855.2:c.1337_1338delinsAT