Canonical Allele Identifier: PA2499238769
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1172231
ClinVar RCV Id: RCV001525915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Val443Phe
CA340132802
NM_001128425.2:c.1327G>T