Allele Registry

Canonical Allele Identifier: PA347858

Gene: MMAA HGNC NCBI

ClinVar RCV:

RCV000203317

ClinVar Variation:

218975

HGVS (amino-acid)	Matching Registered Transcripts
NP_758454.1:p.Gly188Arg	CA347857 NM_172250.3:c.562G>C CA358355248 NM_172250.3:c.562G>A