Canonical Allele Identifier: PA2580151792
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_001121897.1:p.Trp409Arg
CA340133052
NM_001128425.2:c.1225T>C
CA340133053
NM_001128425.2:c.1225T>A