Canonical Allele Identifier: PA916030567
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 182697
ClinVar RCV Id: RCV000160760 RCV000204684 RCV000212699 RCV002053932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Thr6Ile
CA013450
NM_001350651.2:c.17C>T