Canonical Allele Identifier: PA2825305624
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 1686658
ClinVar RCV Id: RCV002331856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Phe296Leu
CA413427643
NM_001011645.3:c.886T>C
CA413427655
NM_001011645.3:c.888T>G
CA413427658
NM_001011645.3:c.888T>A