Canonical Allele Identifier: PA2827558569
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 41754
ClinVar RCV Id: RCV000034671 RCV000144638 RCV000164389 RCV000206141 RCV000515389 RCV000780500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Arg331Cys
CA011638
NM_001350651.2:c.991C>T