Allele Registry

Canonical Allele Identifier: PA915984534

Gene: SH3BP2 HGNC NCBI

ClinVar Allele:

22586

ClinVar RCV:

RCV000007983

ClinVar Variation:

7547

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139328.1:p.Pro475Leu	CA254206 NM_001145856.2:c.1424C>T