Canonical Allele Identifier: PA194959
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 186486
ClinVar RCV Id: RCV000166088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg426Pro
CA012491
NM_001128425.2:c.1277G>C