Canonical Allele Identifier: PA2825227837
Gene: RORC HGNC NCBI
ClinVar RCV:
RCV000652787
ClinVar Variation:
542374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001523.1:p.Ala336Val
CA1095758
NM_001001523.2:c.1007C>T