Allele Registry

Canonical Allele Identifier: PA120771

Gene: AR HGNC NCBI

ClinVar RCV:

RCV000010516

RCV000584561

ClinVar Variation:

9842

492796

HGVS (amino-acid)	Matching Registered Transcripts
NP_000035.2:p.Met781Ile	CA120769 NM_000044.6:c.2343G>T CA413426471 NM_000044.6:c.2343G>A CA413426473 NM_000044.6:c.2343G>C