Canonical Allele Identifier: PA2825026685
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 1030550
ClinVar RCV Id: RCV001332126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Pro283Ser
CA413425770
NM_000044.6:c.847C>T