Canonical Allele Identifier: PA2830364371
Gene: RTTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2262696
ClinVar RCV Id: RCV002778525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775901.3:p.Ser1056Pro
CA402694060
NM_173630.3:c.3166T>C