Canonical Allele Identifier: PA645452883
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 419292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Asn238Thr
CA16617163
NM_001128425.2:c.713A>C