Canonical Allele Identifier: PA186098
Gene: RNF125 HGNC NCBI

Linked Data

ClinVar Variation Id: 183420
ClinVar RCV Id: RCV000162241

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060301.2:p.Met112Ile
CA186097
NM_017831.4:c.336G>A
CA402254591
NM_017831.4:c.336G>C
CA402254592
NM_017831.4:c.336G>T