Allele Registry

Canonical Allele Identifier: PA645423454

Gene: SH3BP2 HGNC NCBI

ClinVar RCV:

RCV000269056

ClinVar Variation:

348593

HGVS (amino-acid)	Matching Registered Transcripts
NP_003014.3:p.Ser505Cys	CA2819599 NM_003023.4:c.1514C>G