Canonical Allele Identifier: PA120778
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9847
ClinVar RCV Id: RCV000010521 RCV003133116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Met276Thr
CA120777
NM_001011645.3:c.827T>C