Canonical Allele Identifier: PA2580152056
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1772772
ClinVar RCV Id: RCV002394428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.His482Tyr
CA340132562
NM_001128425.2:c.1444C>T