Canonical Allele Identifier: PA2826826270
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_001280120.1:p.Ser518Ala
CA340131617
NM_001293191.2:c.1552T>G