Canonical Allele Identifier: PA287876
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 127847
ClinVar RCV Id: RCV000115769 RCV000197617 RCV000212703 RCV000586038 RCV001358471 RCV002477280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ile223Val
CA014073
NM_001128425.2:c.667A>G