Canonical Allele Identifier: PA658668448
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 458360
ClinVar RCV Id: RCV001377727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Leu617Pro
CA413429312
NM_000044.6:c.1850T>C