Canonical Allele Identifier: PA2827427009
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 216890
ClinVar RCV Id: RCV000196772 RCV000499525 RCV000627669 RCV000990850 RCV001269900 RCV002221510 RCV001516905 RCV003927863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Pro392Ser
CA210003
NM_001348061.1:c.1174C>T