Canonical Allele Identifier: PA2826827182
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1000980
ClinVar RCV Id: RCV001297193 RCV001525118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280121.1:p.Val287Ala
CA340133071
NM_001293192.2:c.860T>C