Allele Registry

Canonical Allele Identifier: PA913201401

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000298519

ClinVar Variation:

348585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139327.1:p.Arg412Trp	CA2819399 NM_001145855.2:c.1234C>T