Canonical Allele Identifier: PA186100
Gene: RNF125 HGNC NCBI

Linked Data

ClinVar Variation Id: 183421
ClinVar RCV Id: RCV000162242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060301.2:p.Ser163Leu
CA186099
NM_017831.4:c.488C>T