Canonical Allele Identifier: PA2828149059
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 2224578
ClinVar RCV Id: RCV002683465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351371.1:p.Pro141Leu
CA3195604
NM_001364442.2:c.422C>T