Canonical Allele Identifier: PA2826829456
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 419292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Asn118Thr
CA16617163
NM_001293196.2:c.353A>C