Canonical Allele Identifier: PA2580166100
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2033942
ClinVar RCV Id: RCV002885323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139328.1:p.Gly477Trp
CA356057578
NM_001145856.2:c.1429G>T