Allele Registry

Canonical Allele Identifier: PA112472

Gene: TRIM37 HGNC NCBI

ClinVar RCV:

RCV000049987

ClinVar Variation:

56574

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005207.1:p.Gly322Val	CA144383 NM_001005207.4:c.965G>T