Canonical Allele Identifier: PA2826094334
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_001166986.1:p.Gly38Arg
CA263866
NM_001173515.2:c.112G>C
CA405388176
NM_001173515.2:c.112G>A