Canonical Allele Identifier: PA2827426939
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 492778
ClinVar RCV Id: RCV000582975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Gly248Val
CA413425554
NM_001348061.1:c.743G>T