Canonical Allele Identifier: PA2826830198
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1718437
ClinVar RCV Id: RCV002299824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Gln358Leu
CA056389
NM_001293196.2:c.1073A>T