Allele Registry

Canonical Allele Identifier: PA120742

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010506

ClinVar Variation:

9832

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Leu678Pro	CA120740 NM_000044.6:c.2033T>C