Canonical Allele Identifier: PA2825432091
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 587356
ClinVar RCV Id: RCV000767387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.[Gly475_Thr476insPro;Cys477_Met478delinsAlaGln]
CA913189310
NM_001048174.1:c.1426_1433delinsCCAACAGCCCA