Allele Registry

Canonical Allele Identifier: PA645423414

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000320509

ClinVar Variation:

348576

HGVS (amino-acid)	Matching Registered Transcripts
NP_003014.3:p.Pro166Leu	CA2819192 NM_003023.4:c.497C>T