Canonical Allele Identifier: PA2829673679
Gene: MME HGNC NCBI

Linked Data

ClinVar Variation Id: 1329740
ClinVar RCV Id: RCV001800048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009219.2:p.Tyr232Cys
CA2675241
NM_007288.3:c.695A>G