Canonical Allele Identifier: PA2580483922
Gene: MCEE HGNC NCBI

Linked Data

ClinVar Variation Id: 2101892
ClinVar RCV Id: RCV003026248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115990.3:p.Val134Met
CA347180832
NM_032601.4:c.400G>A