Allele Registry

Canonical Allele Identifier: PA292248

Gene: MTRR HGNC NCBI

ClinVar RCV:

RCV000126886

RCV000266246

RCV000557291

ClinVar Variation:

138306

HGVS (amino-acid)	Matching Registered Transcripts
NP_002445.2:p.Ser257Thr	CA292247 NM_002454.3:c.769T>A