Canonical Allele Identifier: PA2828148767
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 7033
ClinVar RCV Id: RCV000007449 RCV000757493 RCV002512874 RCV003460434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351370.1:p.Ser454Leu
CA254075
NM_001364441.2:c.1361C>T