Canonical Allele Identifier: PA2826823819
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 449417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Arg261Trp
CA059263
NM_001293190.2:c.781C>T
CA645514849
NM_001293190.2:c.780_781delinsTT