Canonical Allele Identifier: PA2580397520
Gene: MMACHC HGNC NCBI

Linked Data

ClinVar Variation Id: 2078686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056321.2:p.Arg89His
CA827673
NM_015506.3:c.266G>A