Canonical Allele Identifier: PA2827426837
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 464794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Gln73_Gln80dup
CA658658998
NM_001348061.1:c.216_239dup
CA2693924000
NM_001348061.1:c.239_240insGCAGCAGCAGCAGCAGCAGCAACA