Allele Registry

Canonical Allele Identifier: PA123399

Gene: TAP2 HGNC NCBI

ClinVar RCV:

RCV000014727

RCV000455533

RCV001517538

RCV001824569

ClinVar Variation:

13724

HGVS (amino-acid)	Matching Registered Transcripts
NP_061313.2:p.Val379Ile	CA123397 NM_018833.3:c.1135G>A