Canonical Allele Identifier: PA101315
Gene: SH3BP2 HGNC NCBI
ClinVar Allele:
22589
ClinVar RCV:
RCV000007986
ClinVar Variation:
7550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116153.1:p.Arg415Pro
CA254209
NM_001122681.1:c.1244G>C