Allele Registry

Canonical Allele Identifier: PA658668483

Gene: AR HGNC NCBI

ClinVar Variation Id: 458362

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Phe726Leu	CA413424259 NM_000044.6:c.2176T>C CA413424271 NM_000044.6:c.2178C>A CA413424274 NM_000044.6:c.2178C>G