Canonical Allele Identifier: PA916029823
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 216890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334993.1:p.Pro392Ser
CA210003
NM_001348064.1:c.1174C>T