Canonical Allele Identifier: PA2829447617
Gene: TRRAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1333827
ClinVar RCV Id: RCV001809042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003487.1:p.Lys2173Arg
CA368285063
NM_003496.4:c.6518A>G