Canonical Allele Identifier: PA2827706810
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 281137
ClinVar RCV Id: RCV000350888 RCV000354466
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340014.1:p.Arg486His
CA8678175
NM_001353085.2:c.1457G>A