Canonical Allele Identifier: PA2826823928
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Arg296Cys
CA011853
NM_001293190.2:c.886C>T