Canonical Allele Identifier: PA2827078054
Gene: CBLB HGNC NCBI

Linked Data

ClinVar Variation Id: 133826
ClinVar RCV Id: RCV000120478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308722.1:p.Ala857Gly
CA157899
NM_001321793.2:c.2570C>G