Allele Registry

Canonical Allele Identifier: PA120768

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010515

ClinVar Variation:

9841

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Glu2Lys	CA120767 NM_000044.6:c.4G>A