Canonical Allele Identifier: PA157900
Gene: CBLB HGNC NCBI

Linked Data

ClinVar Variation Id: 133826
ClinVar RCV Id: RCV000120478
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733762.2:p.Ala901Gly
CA157899
NM_170662.5:c.2702C>G