Canonical Allele Identifier: PA2825921093
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_001139327.1:p.Gly448Trp
CA356057578
NM_001145855.2:c.1342G>T