Canonical Allele Identifier: PA2827556838
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1765930
ClinVar RCV Id: RCV002378759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Leu162Met
CA340134346
NM_001350650.2:c.484C>A