Canonical Allele Identifier: PA645484474
Gene: RTTN HGNC NCBI

Linked Data

ClinVar Variation Id: 373582
ClinVar RCV Id: RCV000413049 RCV003105890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775901.3:p.Asp1843His
CA8994928
NM_173630.3:c.5527G>C