Canonical Allele Identifier: PA2826823961
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 230146
ClinVar Variation Id: 439221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Gly308Arg
CA059784
NM_001293190.2:c.922G>A
CA340134139
NM_001293190.2:c.922G>C