Canonical Allele Identifier: PA2825227892
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_001001523.1:p.His408Tyr
CA1095708
NM_001001523.2:c.1222C>T