Allele Registry

Canonical Allele Identifier: PA2825585724

Gene: SH3BP2 HGNC NCBI

ClinVar Variation Id: 348581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116153.1:p.Asp219Val	CA2819290 NM_001122681.1:c.656A>T