Canonical Allele Identifier: PA915984371
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348572
ClinVar RCV Id: RCV000261336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139328.1:p.Ser204Leu
CA2819177
NM_001145856.2:c.611C>T