Allele Registry

Canonical Allele Identifier: PA645423452

Gene: SH3BP2 HGNC NCBI

ClinVar Variation Id: 348590

HGVS (amino-acid)	Matching Registered Transcripts
NP_003014.3:p.Ser456Leu	CA2819496 NM_003023.4:c.1367C>T