Canonical Allele Identifier: PA2580544540
Gene: RNF113B HGNC NCBI

Linked Data

ClinVar Variation Id: 2266074
ClinVar RCV Id: RCV004116799
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849192.1:p.Pro296Leu
CA7025396
NM_178861.5:c.887C>T