Canonical Allele Identifier: PA2828148561
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 1033922
ClinVar RCV Id: RCV001336469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351370.1:p.Glu162Gly
CA359156839
NM_001364441.2:c.485A>G