Canonical Allele Identifier: PA2825026998
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 2925678
ClinVar RCV Id: RCV003783772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Leu729Ser
CA413424313
NM_000044.6:c.2186T>C