Canonical Allele Identifier: PA287866
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 127840
ClinVar RCV Id: RCV000115760 RCV000212721 RCV000640383 RCV000765173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gln498Arg
CA012941
NM_001128425.2:c.1493A>G