Allele Registry

Canonical Allele Identifier: PA120765

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010514

ClinVar Variation:

9840

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Pro17Ser	CA120764 NM_001011645.3:c.49C>T