Allele Registry

Canonical Allele Identifier: PA913201411

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000007988

RCV000414728

RCV002523913

ClinVar Variation:

7552

372503

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139327.1:p.Gly448Arg	CA254211 NM_001145855.2:c.1342G>C CA16042561 NM_001145855.2:c.1342G>A