Canonical Allele Identifier: PA2830020860
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 3217965
ClinVar RCV Id: RCV004510273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_076915.3:p.Glu162Asp
CA359156841
NM_024010.3:c.486G>C
CA359156842
NM_024010.3:c.486G>T