Canonical Allele Identifier: PA165893
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141595
ClinVar RCV Id: RCV000130180 RCV000456187 RCV000519177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Gly183Asp
CA013822
NM_001128425.2:c.548G>A