Canonical Allele Identifier: PA2827427390
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 216890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334992.1:p.Pro392Ser
CA210003
NM_001348063.1:c.1174C>T