Canonical Allele Identifier: PA2826824632
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 923656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.His523Tyr
CA057048
NM_001293190.2:c.1567C>T