Canonical Allele Identifier: PA2827556832
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_001337579.1:p.Glu160Gly
CA340134367
NM_001350650.2:c.479A>G
CA913187615
NM_001350650.2:c.477_479delinsTGG