Allele Registry

Canonical Allele Identifier: PA645423452

Gene: SH3BP2 HGNC NCBI

ClinVar Allele:

298192

ClinVar RCV:

RCV000264563

RCV002520237

RCV003480615

ClinVar Variation:

348590

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