Canonical Allele Identifier: PA215836
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41764
ClinVar RCV Id: RCV000034681 RCV000123156 RCV000129219 RCV000613933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg274Gln
CA011841
NM_001128425.2:c.821G>A