Canonical Allele Identifier: PA2827556755
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2567652
ClinVar RCV Id: RCV003311347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Phe135Ser
CA340134642
NM_001350650.2:c.404T>C