Allele Registry

Canonical Allele Identifier: PA100215

Gene: HR HGNC NCBI

ClinVar RCV:

RCV000007755

RCV001159828

RCV001723550

RCV004555531

ClinVar Variation:

7330

HGVS (amino-acid)	Matching Registered Transcripts
NP_005135.2:p.Thr1022Ala	CA210692 NM_005144.5:c.3064A>G