Canonical Allele Identifier: PA916072537
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 138306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_076915.3:p.Ser257Thr
CA292247
NM_024010.3:c.769T>A