Canonical Allele Identifier: PA915984382
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348576
ClinVar RCV Id: RCV000320509
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139328.1:p.Pro223Leu
CA2819192
NM_001145856.2:c.668C>T