Canonical Allele Identifier: PA192539
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 185653
ClinVar RCV Id: RCV000165108 RCV000226581 RCV001355674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Pro157Leu
CA013620
NM_001128425.2:c.470C>T