Canonical Allele Identifier: PA2827063950
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_001307916.1:p.Ser253Asn
CA117351
NM_001320987.3:c.758G>A