Allele Registry

Canonical Allele Identifier: PA254902

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010526

ClinVar Variation:

9852

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Leu713Phe	CA254900 NM_000044.6:c.2137C>T