Canonical Allele Identifier: PA2826824629
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1499605
ClinVar RCV Id: RCV002042384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280119.1:p.Ser522Ala
CA340131617
NM_001293190.2:c.1564T>G