Canonical Allele Identifier: PA2825428162
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 449417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041637.1:p.Arg247Trp
CA059263
NM_001048172.1:c.739C>T
CA645514849
NM_001048172.1:c.738_739delinsTT