Canonical Allele Identifier: PA2828149278
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 138294
ClinVar RCV Id: RCV000126874 RCV000382140 RCV001274262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351371.1:p.Pro450Arg
CA292223
NM_001364442.2:c.1349C>G