Canonical Allele Identifier: PA101305
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116153.1:p.Arg415Gln
CA254210
NM_001122681.1:c.1244G>A