Canonical Allele Identifier: PA2827556512
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1750885
ClinVar RCV Id: RCV002357872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.His57Tyr
CA340135427
NM_001350650.2:c.169C>T