Canonical Allele Identifier: PA2827079521
Gene: CBLB HGNC NCBI

Linked Data

ClinVar Variation Id: 133826
ClinVar RCV Id: RCV000120478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308737.1:p.Ala597Gly
CA157899
NM_001321808.2:c.1790C>G