Allele Registry

Canonical Allele Identifier: PA2829447356

Gene: TRRAP HGNC NCBI

ClinVar Allele:

2477593

ClinVar RCV:

RCV003223542

ClinVar Variation:

2499613

HGVS (amino-acid)	Matching Registered Transcripts
NP_003487.1:p.Pro1914Leu	CA368323349 NM_003496.4:c.5741C>T