Canonical Allele Identifier: PA2827557502
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_001337579.1:p.Ser375Asn
CA340131832
NM_001350650.2:c.1124G>A