Canonical Allele Identifier: PA167479
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 142131
ClinVar RCV Id: RCV000130971 RCV003998085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Met201Val
CA013944
NM_001128425.2:c.601A>G