Canonical Allele Identifier: PA2825585688
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_001116153.1:p.Pro166Leu
CA2819192
NM_001122681.1:c.497C>T