Allele Registry

Canonical Allele Identifier: PA645451387

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000489065

ClinVar Variation:

427107

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Arg630Trp	CA413422950 NM_000044.6:c.1888C>T