Canonical Allele Identifier: PA2829448544
Gene: TRRAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1699497
ClinVar RCV Id: RCV002273354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003487.1:p.Leu3308Phe
CA368332128
NM_003496.4:c.9922C>T