Canonical Allele Identifier: PA2827558573
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 819183
ClinVar RCV Id: RCV001011521
ClinVar Variation Id: 933734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Trp332Arg
CA340132615
NM_001350651.2:c.994T>C
CA340132616
NM_001350651.2:c.994T>A