Canonical Allele Identifier: PA2827427186
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 2923962
ClinVar RCV Id: RCV003783520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334992.1:p.Lys17Asn
CA10436207
NM_001348063.1:c.51G>T
CA413423687
NM_001348063.1:c.51G>C