Canonical Allele Identifier: PA2827584538
Gene: TRIM2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337984.1:p.Glu244Val
CA211304
NM_001351055.2:c.731A>T