Canonical Allele Identifier: PA110135
Gene: MCCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1923
ClinVar RCV Id: RCV000002000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071415.1:p.Cys167Arg
CA251969
NM_022132.5:c.499T>C