Canonical Allele Identifier: PA916056725
Gene: TYROBP HGNC NCBI
ClinVar RCV:
RCV000049807
ClinVar Variation:
56394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937758.1:p.Ser39Asn
CA263863
NM_198125.3:c.116G>A