Canonical Allele Identifier: PA2826829106
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 587356
ClinVar RCV Id: RCV000767387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.[Gly475_Thr476insPro;Cys477_Met478delinsAlaGln]
CA913189310
NM_001293195.2:c.1426_1433delinsCCAACAGCCCA