Canonical Allele Identifier: PA112483
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 56569
ClinVar RCV Id: RCV000049982 RCV003415819
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005207.1:p.Leu76Pro
CA144376
NM_001005207.4:c.227T>C