Canonical Allele Identifier: PA174109
Gene: TRIM6-TRIM34 HGNC NCBI

Linked Data

ClinVar Variation Id: 161478
ClinVar RCV Id: RCV000149012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003819.1:p.Ser353Asn
CA174108
NM_001003819.4:c.1058G>A