Canonical Allele Identifier: PA2825585849
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348584
ClinVar RCV Id: RCV000400486 RCV002520236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116153.1:p.Val381Met
CA2819397
NM_001122681.1:c.1141G>A