Canonical Allele Identifier: PA913201411
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7552
ClinVar RCV Id: RCV000007988
ClinVar Variation Id: 372503
ClinVar RCV Id: RCV000414728 RCV002523913
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139327.1:p.Gly448Arg
CA254211
NM_001145855.2:c.1342G>C
CA16042561
NM_001145855.2:c.1342G>A