Canonical Allele Identifier: PA916070592
Gene: MCEE HGNC NCBI

Linked Data

ClinVar Variation Id: 649586
ClinVar RCV Id: RCV000804557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115990.3:p.Arg104His
CA1702606
NM_032601.4:c.311G>A