Canonical Allele Identifier: PA299553
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182689
ClinVar RCV Id: RCV000160752 RCV000200700 RCV000214896 RCV000508179 RCV002478487 RCV004535046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg182His
CA013795
NM_001128425.2:c.545G>A