Canonical Allele Identifier: PA120719
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9822
ClinVar RCV Id: RCV000010496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011645.1:p.Val335Leu
CA120718
NM_001011645.3:c.1003G>T
CA413428104
NM_001011645.3:c.1003G>C