Canonical Allele Identifier: PA2827558767
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1513611
ClinVar RCV Id: RCV002045956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Ser392Thr
CA340131620
NM_001350651.2:c.1174T>A