Canonical Allele Identifier: PA2825305202
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 268093
ClinVar RCV Id: RCV000258807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Ile30Thr
CA10602648
NM_001011645.3:c.89T>C