Canonical Allele Identifier: PA2826823683
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 464736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Thr219Ser
CA058731
NM_001293190.2:c.655A>T
CA340135237
NM_001293190.2:c.656C>G