Canonical Allele Identifier: PA2827705827
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 5246
ClinVar RCV Id: RCV000005558 RCV000729885
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340011.1:p.Ser253Asn
CA117351
NM_001353082.2:c.758G>A