Canonical Allele Identifier: PA916029796
Gene: AR HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334993.1:p.Glu2Lys
CA120767
NM_001348064.1:c.4G>A