Canonical Allele Identifier: PA2826826878
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_001280121.1:p.Glu183Gly
CA340134367
NM_001293192.2:c.548A>G
CA913187615
NM_001293192.2:c.546_548delinsTGG