Canonical Allele Identifier: PA191503
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg241Trp
CA014196
NM_001128425.2:c.721C>T