Allele Registry

Canonical Allele Identifier: PA2580166398

Gene: TRIM77 HGNC NCBI

ClinVar RCV:

RCV004150501

ClinVar Variation:

2302641

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139634.1:p.Gln188Pro	CA382030254 NM_001146162.1:c.563A>C