Allele Registry

Canonical Allele Identifier: PA120744

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010507

ClinVar Variation:

9833

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Thr346Ser	CA120743 NM_001011645.3:c.1037C>G CA413428202 NM_001011645.3:c.1036A>T