Allele Registry

Canonical Allele Identifier: PA2825026714

Gene: AR HGNC NCBI

ClinVar Variation Id: 3061769

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Ser335Arg	CA413426101 NM_000044.6:c.1003A>C CA413426107 NM_000044.6:c.1005C>A CA413426108 NM_000044.6:c.1005C>G