Canonical Allele Identifier: PA2827556368
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2453346
ClinVar RCV Id: RCV003182801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337579.1:p.Trp13Gly
CA340136022
NM_001350650.2:c.37T>G