Allele Registry

Canonical Allele Identifier: PA645446800

Gene: TAP2 HGNC NCBI

ClinVar RCV:

RCV000455618

RCV000987675

ClinVar Variation:

403511

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276972.1:p.Thr665Ala	CA3745742 NM_001290043.2:c.1993A>G