Canonical Allele Identifier: PA2826828489
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1765930
ClinVar RCV Id: RCV002378759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280124.1:p.Leu277Met
CA340134346
NM_001293195.2:c.829C>A