Canonical Allele Identifier: PA645378618
Gene: MCEE HGNC NCBI

Linked Data

ClinVar Variation Id: 336939
ClinVar RCV Id: RCV000372188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115990.3:p.Leu91Met
CA1702615
NM_032601.4:c.271C>A