Canonical Allele Identifier: PA2828148656
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 2178256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351370.1:p.Thr303Ile
CA3195760
NM_001364441.2:c.908C>T