Allele Registry

Canonical Allele Identifier: PA170996

Gene: MTRR HGNC NCBI

ClinVar RCV:

RCV000126880

RCV000144924

RCV000302798

RCV001274263

RCV001812074

ClinVar Variation:

138300

HGVS (amino-acid)	Matching Registered Transcripts
NP_002445.2:p.His595Tyr	CA170995 NM_002454.3:c.1783C>T