Canonical Allele Identifier: PA2827426805
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 2923962
ClinVar RCV Id: RCV003783520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Lys17Asn
CA10436207
NM_001348061.1:c.51G>T
CA413423687
NM_001348061.1:c.51G>C