Allele Registry

Canonical Allele Identifier: PA358792

Gene: MMAA HGNC NCBI

ClinVar RCV:

RCV000210840

ClinVar Variation:

225189

HGVS (amino-acid)	Matching Registered Transcripts
NP_758454.1:p.Met342Arg	CA358791 NM_172250.3:c.1025T>G