Canonical Allele Identifier: PA2580451164
Gene: MTRR HGNC NCBI

Linked Data

ClinVar Variation Id: 2140701
ClinVar RCV Id: RCV003056582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_076915.3:p.Asn218Lys
CA3195661
NM_024010.3:c.654T>G
CA359157191
NM_024010.3:c.654T>A