Canonical Allele Identifier: PA2827427003
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 3061770
ClinVar RCV Id: RCV003983763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Pro381Ser
CA10436384
NM_001348061.1:c.1141C>T