Canonical Allele Identifier: PA916018696
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 492044
ClinVar RCV Id: RCV000583931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280125.1:p.Leu39Pro
CA340135990
NM_001293196.2:c.116T>C