Canonical Allele Identifier: PA913201409
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7548
ClinVar RCV Id: RCV000007984 RCV000486508
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139327.1:p.Pro446Arg
CA254207
NM_001145855.2:c.1337C>G