Canonical Allele Identifier: PA2825738969
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_001123539.1:p.Asp640Ala
CA10584080
NM_001130067.2:c.1919A>C