Canonical Allele Identifier: PA2826826171
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_001280120.1:p.[Gly486_Thr487insPro;Cys488_Met489delinsAlaGln]
CA913189310
NM_001293191.2:c.1459_1466delinsCCAACAGCCCA