Canonical Allele Identifier: PA2580544532
Gene: RNF113B HGNC NCBI

Linked Data

ClinVar Variation Id: 2334329
ClinVar RCV Id: RCV004173109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849192.1:p.Arg98Cys
CA388556368
NM_178861.5:c.292C>T