Canonical Allele Identifier: PA2826824997
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1349009
ClinVar RCV Id: RCV002050959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Arg108Gly
CA340136258
NM_001293191.2:c.322A>G