Canonical Allele Identifier: PA2828624089
Gene: MMAA HGNC NCBI

Linked Data

ClinVar Variation Id: 990263
ClinVar RCV Id: RCV001278249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362573.1:p.His29Arg
CA3095119
NM_001375644.1:c.86A>G