Canonical Allele Identifier: PA2827556821
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 655768
ClinVar RCV Id: RCV000812015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Cys157Trp
CA340134395
NM_001350650.2:c.471C>G