Canonical Allele Identifier: PA2573271072
Gene: TAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484086
ClinVar RCV Id: RCV002037980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061313.2:p.Val423Met
CA363582532
NM_018833.3:c.1267G>A