Canonical Allele Identifier: PA2825428712
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1770733
ClinVar RCV Id: RCV002383390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001041637.1:p.Tyr426Ser
CA340132739
NM_001048172.1:c.1277A>C