Canonical Allele Identifier: PA2829385609
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 2218664
ClinVar RCV Id: RCV002687360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002445.2:p.Ser164Arg
CA3195611
NM_002454.3:c.490A>C
CA359156854
NM_002454.3:c.492T>A
CA359156855
NM_002454.3:c.492T>G