Canonical Allele Identifier: PA2826825345
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 419292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Asn221Thr
CA16617163
NM_001293191.2:c.662A>C