Canonical Allele Identifier: PA2827427529
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 653501
ClinVar RCV Id: RCV000809289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334992.1:p.Cys615Ser
CA413429296
NM_001348063.1:c.1843T>A
CA413429299
NM_001348063.1:c.1844G>C