Canonical Allele Identifier: PA891860338
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 565360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Trp263Arg
CA340134748
NM_001128425.2:c.787T>C
CA340134749
NM_001128425.2:c.787T>A