Canonical Allele Identifier: PA2827557960
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 449417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Arg131Trp
CA059263
NM_001350651.2:c.391C>T
CA645514849
NM_001350651.2:c.390_391delinsTT