Canonical Allele Identifier: PA916070591
Gene: MCEE HGNC NCBI

Linked Data

ClinVar Variation Id: 643880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115990.3:p.Leu79Val
CA1702623
NM_032601.4:c.235C>G