Canonical Allele Identifier: PA915984375
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348575
ClinVar RCV Id: RCV000265353 RCV002520235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139328.1:p.Arg215Trp
CA2819186
NM_001145856.2:c.643C>T