Canonical Allele Identifier: PA2827556610
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 464736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Thr89Ser
CA058731
NM_001350650.2:c.265A>T
CA340135237
NM_001350650.2:c.266C>G