Canonical Allele Identifier: PA2826826839
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 421951
ClinVar RCV Id: RCV000479935 RCV000775777 RCV002525888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Cys170Tyr
CA16617160
NM_001293192.2:c.509G>A