Canonical Allele Identifier: PA2827558619
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 650792
ClinVar RCV Id: RCV000806016
ClinVar Variation Id: 1773353
ClinVar RCV Id: RCV002396927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337580.1:p.Met347Ile
CA340132479
NM_001350651.2:c.1041G>T
CA340132480
NM_001350651.2:c.1041G>C
CA340132482
NM_001350651.2:c.1041G>A