Allele Registry

Canonical Allele Identifier: PA2827065109

Gene: TRIM37 HGNC NCBI

ClinVar RCV:

RCV000350888

RCV000354466

ClinVar Variation:

281137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001307918.1:p.Arg640His	CA8678175 NM_001320989.3:c.1919G>A