Canonical Allele Identifier: PA2827706705
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 56574
ClinVar RCV Id: RCV000049987
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340014.1:p.Gly168Val
CA144383
NM_001353085.2:c.503G>T