Allele Registry

Canonical Allele Identifier: PA120766

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010514

ClinVar Variation:

9840

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Pro549Ser	CA120764 NM_000044.6:c.1645C>T