Canonical Allele Identifier: PA101325
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7552
ClinVar RCV Id: RCV000007988
ClinVar Variation Id: 372503
ClinVar RCV Id: RCV000414728 RCV002523913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116153.1:p.Gly420Arg
CA254211
NM_001122681.1:c.1258G>C
CA16042561
NM_001122681.1:c.1258G>A