Canonical Allele Identifier: PA2828148541
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 966720
ClinVar RCV Id: RCV001241466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351370.1:p.Leu135Phe
CA3195603
NM_001364441.2:c.405A>C
CA359156662
NM_001364441.2:c.405A>T