Canonical Allele Identifier: PA2826094221
Gene: TYROBP HGNC NCBI

Linked Data

ClinVar Variation Id: 595538
ClinVar RCV Id: RCV000731110 RCV003165973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166985.1:p.Pro29Leu
CA9393100
NM_001173514.2:c.86C>T