Canonical Allele Identifier: PA916035702
Gene: TRIM37 HGNC NCBI
ClinVar RCV:
RCV000049987
ClinVar Variation:
56574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340012.1:p.Gly77Val
CA144383
NM_001353083.2:c.230G>T