Canonical Allele Identifier: PA2827077473
Gene: CBLB HGNC NCBI

Linked Data

ClinVar Variation Id: 133826
ClinVar RCV Id: RCV000120478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308717.1:p.Ala901Gly
CA157899
NM_001321788.2:c.2702C>G