Canonical Allele Identifier: PA2826828786
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1000980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Val379Ala
CA340133071
NM_001293195.2:c.1136T>C