Canonical Allele Identifier: PA2826332669
Gene: TRRAP HGNC NCBI

Linked Data

ClinVar Variation Id: 2582431
ClinVar RCV Id: RCV003333417 RCV003333416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231509.1:p.Ala3750Val
CA368343574
NM_001244580.2:c.11249C>T