Canonical Allele Identifier: PA2828080004
Gene: MCCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1061496
ClinVar RCV Id: RCV001371087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350076.1:p.Leu246Pro
CA3297905
NM_001363147.1:c.737T>C