Canonical Allele Identifier: PA916022510
Gene: RTTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305449.1:p.Arg718Thr
CA155010
NM_001318520.2:c.2153G>C