Allele Registry

Canonical Allele Identifier: PA2825926514

Gene: TRIM77 HGNC NCBI

ClinVar RCV:

RCV004154384

ClinVar Variation:

2302055

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139634.1:p.His124Gln	CA382029442 NM_001146162.1:c.372C>A CA382029443 NM_001146162.1:c.372C>G