Allele Registry

Canonical Allele Identifier: PA891865724

Gene: TRIM37 HGNC NCBI

ClinVar RCV:

RCV000350888

RCV000354466

ClinVar Variation:

281137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005207.1:p.Arg640His	CA8678175 NM_001005207.4:c.1919G>A