Canonical Allele Identifier: PA2827426990
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 2921760
ClinVar RCV Id: RCV003782782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334990.1:p.Asp354Glu
CA10436358
NM_001348061.1:c.1062C>A
CA10436359
NM_001348061.1:c.1062C>G