Allele Registry

Canonical Allele Identifier: PA916029823

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000196772

RCV000499525

RCV000627669

RCV000990850

RCV001269900

RCV001516905

RCV002221510

RCV003927863

ClinVar Variation:

216890

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334993.1:p.Pro392Ser	CA210003 NM_001348064.1:c.1174C>T