Allele Registry

Canonical Allele Identifier: PA915979280

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000850295

ClinVar Variation:

689544

HGVS (amino-acid)	Matching Registered Transcripts
NP_056086.2:p.Gly640Cys	CA358469567 NM_015271.5:c.1918G>T