Canonical Allele Identifier: PA2827584189
Gene: TRIM2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337983.1:p.Glu245Val
CA211304
NM_001351054.2:c.734A>T