Canonical Allele Identifier: PA913201381
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525202
ClinVar RCV Id: RCV000629249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139327.1:p.Met40Val
CA2818886
NM_001145855.2:c.118A>G