Allele Registry

Canonical Allele Identifier: PA2829413518

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007985

ClinVar Variation:

7549

HGVS (amino-acid)	Matching Registered Transcripts
NP_003014.3:p.Pro418His	CA254208 NM_003023.4:c.1253C>A CA2586973589 NM_003023.4:c.1253_1254delinsAT