Canonical Allele Identifier: PA2827585147
Gene: TRIM2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337986.1:p.Glu102Val
CA211304
NM_001351057.2:c.305A>T