Canonical Allele Identifier: PA2828149075
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 3217965
ClinVar RCV Id: RCV004510273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351371.1:p.Glu162Asp
CA359156841
NM_001364442.2:c.486G>C
CA359156842
NM_001364442.2:c.486G>T