Allele Registry

Canonical Allele Identifier: PA2825305239

Gene: AR HGNC NCBI

ClinVar RCV:

RCV002016983

ClinVar Variation:

1512041

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Cys48Ser	CA413422864 NM_001011645.3:c.142T>A CA413422868 NM_001011645.3:c.143G>C