Canonical Allele Identifier: PA2827427639
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 3128179
ClinVar RCV Id: RCV004420082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334993.1:p.Pro342Ser
CA10436349
NM_001348064.1:c.1024C>T