Allele Registry

Canonical Allele Identifier: PA2829413506

Gene: SH3BP2 HGNC NCBI

ClinVar Allele:

22589

ClinVar RCV:

RCV000007986

ClinVar Variation:

7550

HGVS (amino-acid)	Matching Registered Transcripts
NP_003014.3:p.Arg415Pro	CA254209 NM_003023.4:c.1244G>C