Canonical Allele Identifier: PA2828149143
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 138306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351371.1:p.Ser257Thr
CA292247
NM_001364442.2:c.769T>A