Canonical Allele Identifier: PA1139683284
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 923365
ClinVar RCV Id: RCV001183964
ClinVar Variation Id: 1508367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Glu303Gly
CA340134367
NM_001128425.2:c.908A>G
CA913187615
NM_001128425.2:c.906_908delinsTGG