Allele Registry

Canonical Allele Identifier: PA2827427139

Gene: AR HGNC NCBI

ClinVar RCV:

RCV002016983

ClinVar Variation:

1512041

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334990.1:p.Cys580Ser	CA413422864 NM_001348061.1:c.1738T>A CA413422868 NM_001348061.1:c.1739G>C