Canonical Allele Identifier: PA658805882
Gene: RORC HGNC NCBI

Linked Data

ClinVar Variation Id: 542374
ClinVar RCV Id: RCV000652787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005051.2:p.Ala357Val
CA1095758
NM_005060.4:c.1070C>T