Canonical Allele Identifier: PA2827426996
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 2690948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Leu369Pro
CA10436371
NM_001348061.1:c.1106T>C