Canonical Allele Identifier: PA2826826900
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Arg189Cys
CA011853
NM_001293192.2:c.565C>T