Canonical Allele Identifier: PA171002
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 138304
ClinVar RCV Id: RCV000126884 RCV000144927 RCV000405120 RCV001274256
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002445.2:p.Ser175Leu
CA171001
NM_002454.3:c.524C>T