Canonical Allele Identifier: PA196918
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 187172
ClinVar RCV Id: RCV000166871 RCV000640377 RCV002286709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Arg474His
CA012768
NM_001128425.2:c.1421G>A