Canonical Allele Identifier: PA092021
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036354.1:p.Arg179His
CA013795
NM_012222.3:c.536G>A