Canonical Allele Identifier: PA891860351
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 571385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ser298Arg
CA21837059
NM_001128425.2:c.894C>G
CA340134424
NM_001128425.2:c.894C>A
CA340134431
NM_001128425.2:c.892A>C