Canonical Allele Identifier: PA2829447398
Gene: TRRAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1806308
ClinVar RCV Id: RCV002470592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003487.1:p.Ala1970Thr
CA368325311
NM_003496.4:c.5908G>A