Canonical Allele Identifier: PA144384
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 56574
ClinVar RCV Id: RCV000049987
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056109.1:p.Gly322Val
CA144383
NM_015294.6:c.965G>T