Canonical Allele Identifier: PA2828149097
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 2192784
ClinVar RCV Id: RCV002623790 RCV004070646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351371.1:p.Val180Met
CA3195629
NM_001364442.2:c.538G>A