Canonical Allele Identifier: PA2827426984
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 3128179
ClinVar RCV Id: RCV004420082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Pro342Ser
CA10436349
NM_001348061.1:c.1024C>T