Canonical Allele Identifier: PA2828148250
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 138294
ClinVar RCV Id: RCV000126874 RCV000382140 RCV001274262
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351369.1:p.Pro450Arg
CA292223
NM_001364440.2:c.1349C>G