Canonical Allele Identifier: PA2826824709
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41762
ClinVar RCV Id: RCV000034679 RCV001300424 RCV001189986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Ser10Gly
CA011818
NM_001293191.2:c.28A>G