Allele Registry

Canonical Allele Identifier: PA104641

Gene: MMAA HGNC NCBI

ClinVar RCV:

RCV000203388

ClinVar Variation:

218979

HGVS (amino-acid)	Matching Registered Transcripts
NP_758454.1:p.Arg359Gln	CA347905 NM_172250.3:c.1076G>A