Canonical Allele Identifier: PA120693
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9809
ClinVar RCV Id: RCV000010483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Ser116Asn
CA120692
NM_001011645.3:c.347G>A