Allele Registry

Canonical Allele Identifier: PA2825305444

Gene: AR HGNC NCBI

ClinVar Variation Id: 458362

HGVS (amino-acid)	Matching Registered Transcripts
NP_001011645.1:p.Phe194Leu	CA413424259 NM_001011645.3:c.580T>C CA413424271 NM_001011645.3:c.582C>A CA413424274 NM_001011645.3:c.582C>G