Canonical Allele Identifier: PA2825227810
Gene: RORC HGNC NCBI

Linked Data

ClinVar Variation Id: 1929489
ClinVar RCV Id: RCV002618679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001523.1:p.Thr285Ser
CA342014025
NM_001001523.2:c.854C>G
CA342014036
NM_001001523.2:c.853A>T