Allele Registry

Canonical Allele Identifier: PA2826332033

Gene: TRRAP HGNC NCBI

ClinVar Allele:

2477593

ClinVar RCV:

RCV003223542

ClinVar Variation:

2499613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001231509.1:p.Pro1932Leu	CA368323349 NM_001244580.2:c.5795C>T