Canonical Allele Identifier: PA2826332514
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_001231509.1:p.Leu3337Phe
CA368332128
NM_001244580.2:c.10009C>T