Canonical Allele Identifier: PA915979195
Gene: TRIM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 83303
ClinVar RCV Id: RCV000074302
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056086.2:p.Glu254Val
CA211304
NM_015271.5:c.761A>T