Canonical Allele Identifier: PA2828147976
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 354343
ClinVar RCV Id: RCV000322148 RCV000811882 RCV003168548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351369.1:p.Arg70Cys
CA3195516
NM_001364440.2:c.208C>T