Allele Registry

Canonical Allele Identifier: PA645429938

Gene: TRIM2 HGNC NCBI

ClinVar RCV:

RCV000235081

ClinVar Variation:

243075

HGVS (amino-acid)	Matching Registered Transcripts
NP_056086.2:p.Asp667Ala	CA10584080 NM_015271.5:c.2000A>C