Canonical Allele Identifier: PA2827556618
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1756723
ClinVar RCV Id: RCV002364870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Val91Gly
CA340134925
NM_001350650.2:c.272T>G