Allele Registry

Canonical Allele Identifier: PA120745

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010507

ClinVar Variation:

9833

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Thr878Ser	CA120743 NM_000044.6:c.2633C>G CA413428202 NM_000044.6:c.2632A>T