Canonical Allele Identifier: PA915987980
Gene: RORC HGNC NCBI

Linked Data

ClinVar Variation Id: 656474
ClinVar RCV Id: RCV000812904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005051.2:p.His429Tyr
CA1095708
NM_005060.4:c.1285C>T