Canonical Allele Identifier: PA2826826337
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 230457
ClinVar RCV Id: RCV000214239 RCV000482082 RCV000699073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Ala7Thr
CA057571
NM_001293192.2:c.19G>A