Canonical Allele Identifier: PA2573291257
Gene: MCEE HGNC NCBI

Linked Data

ClinVar Variation Id: 1513623
ClinVar RCV Id: RCV002026260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115990.3:p.Lys156Glu
CA49687432
NM_032601.4:c.466A>G