Canonical Allele Identifier: PA2828149106
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 1436051
ClinVar RCV Id: RCV002001993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351371.1:p.Asp197Asn
CA3195643
NM_001364442.2:c.589G>A