Canonical Allele Identifier: PA2580152052
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1772769
ClinVar RCV Id: RCV002394425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.His482Asp
CA340132563
NM_001128425.2:c.1444C>G