Canonical Allele Identifier: PA2825432033
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 998698
ClinVar RCV Id: RCV001294588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041639.1:p.Val458Leu
CA21835704
NM_001048174.1:c.1372G>C