Canonical Allele Identifier: PA913200894
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 587356
ClinVar RCV Id: RCV000767387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.[Gly503_Thr504insPro;Cys505_Met506delinsAlaGln]
CA913189310
NM_001128425.2:c.1510_1517delinsCCAACAGCCCA