Canonical Allele Identifier: PA915991626
Gene: MME HGNC NCBI

Linked Data

ClinVar Variation Id: 242839
ClinVar RCV Id: RCV000234863 RCV001814126
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009220.2:p.Cys621Arg
CA10584007
NM_007289.4:c.1861T>C