Canonical Allele Identifier: PA2826829963
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1000980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Val287Ala
CA340133071
NM_001293196.2:c.860T>C