Allele Registry

Canonical Allele Identifier: PA2827705838

Gene: TRIM37 HGNC NCBI

ClinVar RCV:

RCV000049987

ClinVar Variation:

56574

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340011.1:p.Gly288Val	CA144383 NM_001353082.2:c.863G>T