Allele Registry

Canonical Allele Identifier: PA2827705943

Gene: TRIM37 HGNC NCBI

ClinVar RCV:

RCV000350888

RCV000354466

ClinVar Variation:

281137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340011.1:p.Arg606His	CA8678175 NM_001353082.2:c.1817G>A