Canonical Allele Identifier: PA2826826218
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2040099
ClinVar RCV Id: RCV002886254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Ser501Asn
CA340131832
NM_001293191.2:c.1502G>A