Canonical Allele Identifier: PA112472
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 56574
ClinVar RCV Id: RCV000049987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005207.1:p.Gly322Val
CA144383
NM_001005207.4:c.965G>T