Canonical Allele Identifier: PA2827556917
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2096288
ClinVar RCV Id: RCV003014101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Cys189Ser
CA340134005
NM_001350650.2:c.566G>C
CA340134011
NM_001350650.2:c.565T>A