Allele Registry

Canonical Allele Identifier: PA170999

Gene: MTRR HGNC NCBI

ClinVar RCV:

RCV000126870

RCV000144925

RCV000317483

RCV001274260

ClinVar Variation:

138291

HGVS (amino-acid)	Matching Registered Transcripts
NP_002445.2:p.Lys350Arg	CA170998 NM_002454.3:c.1049A>G