Canonical Allele Identifier: PA2829385702
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 2056397
ClinVar RCV Id: RCV002938538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002445.2:p.Asn218His
CA359157186
NM_002454.3:c.652A>C