Canonical Allele Identifier: PA299559
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg294Cys
CA014535
NM_001128425.2:c.880C>T