Canonical Allele Identifier: PA2829450594
Gene: TYROBP HGNC NCBI

Linked Data

ClinVar Variation Id: 2052028
ClinVar RCV Id: RCV002932413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003323.1:p.Asp32Tyr
CA9393126
NM_003332.4:c.94G>T