Canonical Allele Identifier: PA155011
Gene: RTTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130183
ClinVar RCV Id: RCV000118212 RCV000949027 RCV003982891 RCV002498530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775901.3:p.Arg1630Thr
CA155010
NM_173630.3:c.4889G>C