Canonical Allele Identifier: PA2826332307
Gene: TRRAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1371450
ClinVar RCV Id: RCV001899575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231509.1:p.Thr2628Met
CA4361275
NM_001244580.2:c.7883C>T