Canonical Allele Identifier: PA2580555986
Gene: TYROBP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937758.1:p.Asp32Tyr
CA9393126
NM_198125.3:c.94G>T