Canonical Allele Identifier: PA2826331796
Gene: TRRAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1806315
ClinVar RCV Id: RCV002470599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231509.1:p.Glu1224Lys
CA368301758
NM_001244580.2:c.3670G>A