Canonical Allele Identifier: PA2827078677
Gene: CBLB HGNC NCBI

Linked Data

ClinVar Variation Id: 133826
ClinVar RCV Id: RCV000120478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308727.1:p.Ala808Gly
CA157899
NM_001321798.2:c.2423C>G