Canonical Allele Identifier: PA913201407
Gene: SH3BP2 HGNC NCBI
ClinVar RCV:
RCV000007983
ClinVar Variation:
7547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139327.1:p.Pro446Leu
CA254206
NM_001145855.2:c.1337C>T