Canonical Allele Identifier: PA916072526
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 391669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_076915.3:p.Ala149Val
CA3195607
NM_024010.3:c.446C>T