Canonical Allele Identifier: PA2828148549
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 391669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351370.1:p.Ala149Val
CA3195607
NM_001364441.2:c.446C>T