Canonical Allele Identifier: PA167931
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Thr232Ala
CA014124
NM_001128425.2:c.694A>G