Canonical Allele Identifier: PA120788
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9857
ClinVar RCV Id: RCV000010531 RCV000010532 RCV001851781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Gly744Val
CA120786
NM_000044.6:c.2231G>T