Canonical Allele Identifier: PA104671
Gene: MMAA HGNC NCBI

Linked Data

ClinVar Variation Id: 218977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758454.1:p.Gly218Glu
CA347896
NM_172250.3:c.653G>A