Canonical Allele Identifier: PA2828149121
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 2150753
ClinVar RCV Id: RCV003071955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351371.1:p.Asn218Asp
CA359157187
NM_001364442.2:c.652A>G