Canonical Allele Identifier: PA1139684495
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 988308
ClinVar RCV Id: RCV001269573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Asn79Lys
CA413429273
NM_001011645.3:c.237T>A
CA413429274
NM_001011645.3:c.237T>G