Canonical Allele Identifier: PA2580407487
Gene: TAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2142212
ClinVar RCV Id: RCV003076259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061313.2:p.Arg354Cys
CA136999884
NM_018833.3:c.1060C>T