Canonical Allele Identifier: PA2830070658
Gene: RNF135 HGNC NCBI

Linked Data

ClinVar Variation Id: 3155040
ClinVar RCV Id: RCV004454388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115698.3:p.Ser271Asn
CA8485342
NM_032322.4:c.812G>A