Canonical Allele Identifier: PA2827427635
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 3061769
ClinVar RCV Id: RCV003983762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334993.1:p.Ser335Arg
CA413426101
NM_001348064.1:c.1003A>C
CA413426107
NM_001348064.1:c.1005C>A
CA413426108
NM_001348064.1:c.1005C>G