Canonical Allele Identifier: PA092041
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Arg238Trp
CA014196
NM_012222.3:c.712C>T