Canonical Allele Identifier: PA2826825859
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1754203
ClinVar RCV Id: RCV002364414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280120.1:p.Trp392Arg
CA340133052
NM_001293191.2:c.1174T>C
CA340133053
NM_001293191.2:c.1174T>A