Canonical Allele Identifier: PA645429938
Gene: TRIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 243075
ClinVar RCV Id: RCV000235081
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Amino-acid Alleles

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