Allele Registry

Canonical Allele Identifier: PA120694

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010483

ClinVar Variation:

9809

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Ser648Asn	CA120692 NM_000044.6:c.1943G>A