Canonical Allele Identifier: PA263868
Gene: TYROBP HGNC NCBI

Linked Data

ClinVar Variation Id: 56396
ClinVar RCV Id: RCV000049809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003323.1:p.Gly49Arg
CA263866
NM_003332.4:c.145G>C
CA405388176
NM_003332.4:c.145G>A