Allele Registry

Canonical Allele Identifier: PA254905

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010527

ClinVar Variation:

9853

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Gly578Arg	CA254903 NM_000044.6:c.1732G>A CA413422851 NM_000044.6:c.1732G>C