Canonical Allele Identifier: PA645453128
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 433935
ClinVar RCV Id: RCV000502805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121897.1:p.Cys297Phe
CA340134438
NM_001128425.2:c.890G>T