Canonical Allele Identifier: PA2827557613
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1735139
ClinVar RCV Id: RCV002355232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.His9Tyr
CA340136244
NM_001350651.2:c.25C>T