Allele Registry

Canonical Allele Identifier: PA104718

Gene: MMAA HGNC NCBI

ClinVar Allele:

18198

ClinVar RCV:

RCV000003309

ClinVar Variation:

3159

HGVS (amino-acid)	Matching Registered Transcripts
NP_758454.1:p.Tyr207Cys	CA252607 NM_172250.3:c.620A>G