Allele Registry

Canonical Allele Identifier: PA2827065510

Gene: TRIM37 HGNC NCBI

ClinVar RCV:

RCV000049987

ClinVar Variation:

56574

HGVS (amino-acid)	Matching Registered Transcripts
NP_001307919.1:p.Gly200Val	CA144383 NM_001320990.3:c.599G>T