Canonical Allele Identifier: PA645423418
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348582
ClinVar RCV Id: RCV000292514 RCV004021961 RCV003238756
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003014.3:p.Gly313Arg
CA2819361
NM_003023.4:c.937G>A
CA356056447
NM_003023.4:c.937G>C