Canonical Allele Identifier: PA1139683770
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 963489
ClinVar RCV Id: RCV001237521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Ala459Thr
CA340132703
NM_001128425.2:c.1375G>A