Canonical Allele Identifier: PA2828148831
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 2236900
ClinVar RCV Id: RCV002718905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351370.1:p.Asn528Thr
CA3195991
NM_001364441.2:c.1583A>C