Allele Registry

Canonical Allele Identifier: PA2825585892

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV002052435

ClinVar Variation:

1526420

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116153.1:p.Gly420Ala	CA356057584 NM_001122681.1:c.1259G>C