Allele Registry

Canonical Allele Identifier: PA104671

Gene: MMAA HGNC NCBI

ClinVar RCV:

RCV000203378

RCV002509299

ClinVar Variation:

218977

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