Canonical Allele Identifier: PA2826825568
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Arg292Cys
CA011853
NM_001293191.2:c.874C>T