Canonical Allele Identifier: PA169444
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142801
ClinVar RCV Id: RCV000132221 RCV000640388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg309His
CA014653
NM_001128425.2:c.926G>A