Canonical Allele Identifier: PA2827426999
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 2926075
ClinVar RCV Id: RCV003786361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Pro375Ser
CA413426348
NM_001348061.1:c.1123C>T