Canonical Allele Identifier: PA2827706962
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 56569
ClinVar RCV Id: RCV000049982 RCV003415819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340015.1:p.Leu76Pro
CA144376
NM_001353086.2:c.227T>C