Canonical Allele Identifier: PA312697
Gene: MCEE HGNC NCBI

Linked Data

ClinVar Variation Id: 203810
ClinVar RCV Id: RCV000203412 RCV000593824 RCV002282020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115990.3:p.Arg143Cys
CA312696
NM_032601.4:c.427C>T