Allele Registry

Canonical Allele Identifier: PA104698

Gene: MMAA HGNC NCBI

ClinVar RCV:

RCV000203404

ClinVar Variation:

218971

HGVS (amino-acid)	Matching Registered Transcripts
NP_758454.1:p.Leu89Pro	CA347910 NM_172250.3:c.266T>C