Canonical Allele Identifier: PA913199280
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 618732
ClinVar RCV Id: RCV000757494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002445.2:p.Asp203Tyr
CA359157086
NM_002454.3:c.607G>T