Canonical Allele Identifier: PA2825227821
Gene: RORC HGNC NCBI

Linked Data

ClinVar Variation Id: 2053961
ClinVar RCV Id: RCV002919208
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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