Canonical Allele Identifier: PA094419
Gene: RNF135 HGNC NCBI
ClinVar RCV:
RCV000001029
ClinVar Variation:
978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115698.3:p.Arg286His
CA114685
NM_032322.4:c.857G>A