Canonical Allele Identifier: PA915971500
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 819558
ClinVar RCV Id: RCV001012208 RCV001860697
ClinVar Variation Id: 1332084
ClinVar RCV Id: RCV001804600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Met524Ile
CA340131745
NM_001128425.2:c.1572G>T
CA340131747
NM_001128425.2:c.1572G>C
CA340131749
NM_001128425.2:c.1572G>A