Canonical Allele Identifier: PA2828881331
Gene: UCP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2191040
ClinVar RCV Id: RCV002616705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368879.1:p.Val51Met
CA224505781
NM_001381950.1:c.151G>A