Canonical Allele Identifier: PA645452239
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 428281
ClinVar RCV Id: RCV000491960 RCV001323975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Pro157Ser
CA340136006
NM_001128425.2:c.469C>T