Canonical Allele Identifier: PA2827427384
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 3061770
ClinVar RCV Id: RCV003983763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334992.1:p.Pro381Ser
CA10436384
NM_001348063.1:c.1141C>T