Canonical Allele Identifier: PA293961
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 140877
ClinVar RCV Id: RCV000129105 RCV000196778 RCV000212706 RCV000515198 RCV001262379 RCV001353906 RCV003313780 RCV004532545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg245His
CA014226
NM_001128425.2:c.734G>A