Canonical Allele Identifier: PA1139670003
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 988302
ClinVar RCV Id: RCV001269561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Ser741Phe
CA413424512
NM_000044.6:c.2222C>T