Canonical Allele Identifier: PA2825026632
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 2660770
ClinVar RCV Id: RCV003438443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000035.2:p.Asp154Glu
CA413424935
NM_000044.6:c.462C>A
CA413424936
NM_000044.6:c.462C>G