ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828881052
Gene: UCP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
130697
ClinVar RCV Id:
RCV000118811
RCV001682828
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001368873.1:p.Ala55Val
CA155899
NM_001381944.1:c.164C>T