Canonical Allele Identifier: PA2580540654
Gene: TRIM69 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892030.3:p.Leu124Arg
CA7536434
NM_182985.5:c.371T>G