Canonical Allele Identifier: PA2828148180
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 138291
ClinVar RCV Id: RCV000126870 RCV000144925 RCV000317483 RCV001274260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351369.1:p.Lys350Arg
CA170998
NM_001364440.2:c.1049A>G