Canonical Allele Identifier: PA913201397
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348582
ClinVar RCV Id: RCV000292514 RCV004021961 RCV003238756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139327.1:p.Gly341Arg
CA2819361
NM_001145855.2:c.1021G>A
CA356056447
NM_001145855.2:c.1021G>C