Canonical Allele Identifier: PA2825227821
Gene: RORC HGNC NCBI
ClinVar RCV:
RCV002919208
ClinVar Variation:
2053961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001523.1:p.His301Arg
CA342013109
NM_001001523.2:c.902A>G