Canonical Allele Identifier: PA2828149076
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 1033922
ClinVar RCV Id: RCV001336469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351371.1:p.Glu162Gly
CA359156839
NM_001364442.2:c.485A>G