Canonical Allele Identifier: PA913201398
Gene: SH3BP2 HGNC NCBI
ClinVar RCV:
RCV000352048
ClinVar Variation:
348583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139327.1:p.Gly403Arg
CA2819390
NM_001145855.2:c.1207G>A
CA356057201
NM_001145855.2:c.1207G>C