Canonical Allele Identifier: PA645423414
Gene: SH3BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348576
ClinVar RCV Id: RCV000320509
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003014.3:p.Pro166Leu
CA2819192
NM_003023.4:c.497C>T