Canonical Allele Identifier: PA174459
Gene: TRRAP HGNC NCBI

Linked Data

ClinVar Variation Id: 161616
ClinVar RCV Id: RCV000149152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003487.1:p.Gln2800Arg
CA174458
NM_003496.4:c.8399A>G