Canonical Allele Identifier: PA916035700
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 5246
ClinVar RCV Id: RCV000005558 RCV000729885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340012.1:p.Ser42Asn
CA117351
NM_001353083.2:c.125G>A