Canonical Allele Identifier: PA916035702
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_001340012.1:p.Gly77Val
CA144383
NM_001353083.2:c.230G>T