Canonical Allele Identifier: PA2826830207
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1772772
ClinVar RCV Id: RCV002394428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.His362Tyr
CA340132562
NM_001293196.2:c.1084C>T